REVISIONS

REV ECN # IMPLEMENTED BY / DATE APPROVED BY / DATE

P8 not released
A 20131470 Jan Hertzen 07-24-2013 Troy Hinzman 7/24/13
B 20131619 Jan Hertzen 08-08-2013 Troy Hinzman 8/08/13

TEXT FOR
CENTURION® VISION SYSTEM
OPERATOR'S MANUAL

1. Inspect per Generic Q-Manual. 1

2. Safety Critical Component.
3. This drawing contains a total of 1 Control Dimension Number. 0
4. If only text is ordered, shrink wrap pages with cardboard backing.

The information contained within this document is confidential and proprietary to Alcon Research, Ltd.
This information shall not be reproduced or further disclosed, in whole or in part, to anyone other than
Alcon employees without prior written consent from Alcon Research Ltd.

SHEET 1 of 195

BY DATE TITLE
Jan Hertzen 3/22/12 TEXT, MANUAL,
CHECKED
OP CENTURION
Kurt Leukanech 3/22/12
IRVINE, CA 92618-3818
APPROVED DWG NO. REV
Kurt Leukanech 3/22/12 905-2150-001 B

FOR REFERENCE ONLY

 ®

®
Operator's Manual

EC REP
Manufacturer:
Alcon Laboratories, Inc. Alcon Laboratories (UK) Ltd.
6201 South Freeway Frimley Business Park
Fort Worth, Texas 76134-2099 Frimley, Camberley
U.S.A. Surrey, GU16 7SR, United Kingdom

Produced By:
Alcon Research, Ltd.
15800 Alton Parkway
Irvine, California 92618-3818
U.S.A.

Telephone: 949/753-1393 Directive 93/42/EEC

800/832-7827
FAX: 949/753-6614

8065751772 B CATALOG NUMBER

905-2150-001 B TEXT ONLY

© 2013 Novartis a Novartis company

FOR REFERENCE ONLY

 Centurion® Vision System Operator's Manual
8065751772

MANUAL REVISION RECORD

DATE REVISION ECN NUMBER AND DESCRIPTION

July 2013 A 20131470 - Initial release of Centurion® Vision System Operator's

Manual with catalog number 8065751772, and 905-2150-001 text
(applies to Centurion® Vision System consoles with software version
REL_02.01).

August, 2013 B 20131619 - Several pages updated with new touchscreen pictures.
Update of AutoSert® IOL feature caused several changes on many
pages. Applies to Centurion® Vision System consoles with software
version REL_02.01. Before changes, pages directly affected are i, ii,
iii, viii, xi, 1.6, 1.8, 1.10, 1.16, 1.17, 1.24, 1.26, 2.5, 2.7, 2.11, 2.12,
2.14, 2.18, 2.22, 2.23, 2.25, 2.26, 2.28, 2.33, 2.44, 2.48, 2.50, 2.51,
2.53, 2.55, 2.56, 2.61, 2.63, 2.68, 2.69, 2.75, 2.83, 2.85, 2.86, 3.5, 3.10,
3.11, 3.12, 4.3, 4.6, 5.1, 5.11, 5.12, 5.15, 5.16, 5.17, 5.18, 6.2, 6.3, 6.4,
7.1, 7.2, 7.3, 7.4.

END USER LICENSE AGREEMENT:

This product contains software licensed from Microsoft Corporation.

Cycoloy and Lexan are registered trademarks of Sabic Innovative Plastics IP

ii
FOR REFERENCE ONLY 8065751772
 TABLE OF CONTENTS

SECTION ONE - GENERAL INFORMATION PAGE #

Overview of Centurion Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.1
®

Key Features of the Centurion® Vision System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.2

Indications for Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Intended Use Environments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Phaco Handpiece Note. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Trademark Note . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Abbreviation Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
Accessory Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.3
User Information – Environmental Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4
Universal Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4
EMC Statements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.4
Equipment Contains Radio Transmitters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.8
USA - Federal Communications Commission (FCC). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.8
Canada - Industry of Canada (IC). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.9
Europe - R&TTE Directive 99/5/EC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.10
Japan. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.10
Warnings and Cautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.11
Phaco Handpiece Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.13
Phaco Handpiece Tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.14
Ultraflow™* II I/A Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.15
Recommended Vacuum Range for I/A Tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.15
Centurion® Vitrectomy Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.15
INTREPID® AutoSert® IOL Injector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.16
Aspiration/Vacuum Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.16
Presurgical Check-out Tests. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.17
IV Pole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.17
Footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.17
Occlusion Tones. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18
Vacuum Tone. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18
Cautery, Diathermy, Coagulation Definition. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.18
Coagulation Function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.19
VideOverlay System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.20
Consumable Paks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.21
Product Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.22
Limited Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.23
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.24
Abbreviations Used with the Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.24
Icons Used with the Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.25
Labeling On Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.26
Coagulation Power Outputs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.28
Summary of Alcon Default Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.29

8065751772 iii
FOR REFERENCE ONLY
SECTION TWO - DESCRIPTION PAGE #
Description of Centurion Vision System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.1
®

Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.1
Trademark Note . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.1
Centurion® Vision System Console and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.2
Description of Console. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.2
Fluidics Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.2
Front Display Panel and Touch Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3
Adjustable Instrument Tray. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.3
Front Panel Connectors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3
Standby Power Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4
Accessory Drawer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4
Audio Speakers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4
Locking Caster Wheels. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Handle Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Equipotential Ground Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
AC Power Cord Hanger . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Primary AC Power Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Footswitch Hanger / Charging Station. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Input/Output (I/O) Connector Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Rotating Work Surface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6
Fluidics Administration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7
Power IV Pole and Hanger for Gravity Fluidics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7
Bag Bay for Active Fluidics™ Technology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7
Description of Footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.8
Footpedal Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.9
Toe Switch Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.11
Footswitch Status LEDs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13
Changing Footswitch Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13
Pairing Footswitch with Centurion® System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13
Footswitch Floor Security. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.14
Cabled Footswitch Connectors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.14
Description of IR Remote Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.15
Remote Control Keys and Buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.15
Remote Control Batteries. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.17
Select Remote Control Channel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.18
Handpieces, Tips, and Infusion Sleeves. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
Phaco Handpieces. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
TurboSonics® Family of Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.21
Infusion Sleeves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.22
UltraFlow™* II I/A Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.23
INTREPID® AutoSert® IOL Injector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.24
Centurion® UltraVit® Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.26
INTREPID® Capsulotomy Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.27
Bipolar Coagulation Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.27
Fluidic Management System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28

iv
FOR REFERENCE ONLY 8065751772
 Consumable Pack Configurations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.29
Custom Pak™* Surgical Procedure Pack Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . 2.29
Centurion® Fluidic Management System Paks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.30
VideOverlay System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.31
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.31
Setup For Standard VideOverlay System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.32

Centurion® Vision System Operator Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.35

Front Display Panel and Touch Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.35
Setup Screen and Its Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.36
Status Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.36
Doctor Name Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.37
Manage Doctors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Procedure Type Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.40
Remote Control Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.42
Front Panel Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.42
Footswitch Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.43
Cumulative Dissipated Energy (CDE). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.43
SGS Pairing Indicator. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.43
Setup Status Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.45
Custom Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.46
Custom / Doctor Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
Custom / Doctor Settings / General Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
Custom / Doctor Settings / Fluidics Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.48
Custom / Doctor Settings / Footswitch Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.49
Custom / Doctor Settings / Sounds Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Custom / Doctor Settings / SGS Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Custom / Doctor Settings / Advanced Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.51
Custom / Save. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.52
Custom / Save As . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.52
Custom / System Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53
Custom / System Settings / General Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53
Custom / System Settings / Wireless Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Custom / Backup/Restore. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Custom / Backup/Restore / Backup Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Custom / Backup/Restore / Restore Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Custom / Procedure Builder. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.57
Custom / About. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Custom / View Events. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Custom / Shutdown System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.61
Setup Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62
Prime FMS / Prime Bag Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62
Fill Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62
Test Handpiece Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.63
PEL Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.63
Test ICD Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.63
Surgery Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.63

8065751772 v
FOR REFERENCE ONLY
 Surgery Screen and Its Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64
Status Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64
Surgery Window. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64
Surgery Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.65
Fluidics Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.68
Surgery Window with Phaco Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Surgery Window with I/A Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Surgery Window with AutoSert® Injector Step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74
Surgery Window with Coagulation Step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74
Surgery Window with AnteriorVitrectomy Step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.75
Surgery Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.76
Setup Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.77
Procedural Step Buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.77
Stationary Step Buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.77

Surgery Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.78

Phaco Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.78
Power/Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.78
Phaco Timing Configurations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.79
Irrigation/Aspiration Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.82
Vacuum Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.83
Aspiration Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.83
Using Fill Step for Irrigation/Aspiration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.83
AutoSert® IOL Injector Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.84
Coagulation (Coag) Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.87
Anterior Vitrectomy Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.89
Anterior Vitrectomy (Anterior Vit). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.90
Epinucleus Removal (Epi Removal). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.90
Irrigation/Aspiration Cut (I/A Cut). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91
Peripheral Iridotomy (Peripheral Irid) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91
Visco Aspiration (Visco Asp). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.92

SECTION THREE - OPERATING INSTRUCTIONS PAGE #

Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Power Up Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Shut Down Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.1
Initial System Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.2
Centurion® FMS Pack Setup Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3
Phaco Handpiece Setup and Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5
Irrigation/Aspiration Handpiece Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.9
INTREPID® AutoSert® IOL Injector Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.10
Centurion® ULTRAVIT® Probe Setup (using Vitrectomy Setup dialog). . . . . . . . . . . . . . . . . . . . . . 3.13
Centurion® ULTRAVIT® Probe Setup (without using Vitrectomy Setup dialog). . . . . . . . . . . . . . . 3.16
Coagulation Handpiece Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.17
INTREPID® Capsulotomy Device Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.17

vi
FOR REFERENCE ONLY 8065751772
SECTION FOUR - CARE AND MAINTENANCE PAGE #
Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.1
Upon Completion of the Day's Surgery Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2
Care and Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.4
Sterilization Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.5
Fuse Replacement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.6
Packing the Centurion® System for Transit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.7
Setting Up the Reconstitution Rack. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.8

SECTION FIVE - TROUBLESHOOTING PAGE #

Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.1
System Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.1
Observed Conditions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.5
Advisories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5.10

SECTION SIX - ACCESSORIES AND PARTS PAGE #

Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.1
Catalog Items . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.2

SECTION SEVEN - INDEX PAGE #

Alphabetized Listing of Topics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7.1

8065751772 vii
FOR REFERENCE ONLY
 LIST OF FIGURES

FIGURE# TITLE PAGE #

Figure 1-1 The Centurion Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.1
®

Figure 1-2 Icons Used with the Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.25
Figure 1-3A Labeling on Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.26
Figure 1-3B Labeling on Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.27
Figure 1-4 Coagulation Power Outputs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.28

Figure 2-1 The Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.2

Figure 2-2 The Front Panel Connectors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3
Figure 2-3 Rear and Side Panels. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4
Figure 2-4 Rotating Work Surface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6
Figure 2-5 The Centurion® System Footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.8
Figure 2-6 Diagram of Footpedal Positions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.9
Figure 2-7 Doctor Settings Dialog Screen - Footswitch Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.10
Figure 2-8 Doctor Settings Dialog Screen - Button Assignment Selections . . . . . . . . . . . . . . . 2.10
Figure 2-9 Bottom of Centurion® System Footswitch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.14
Figure 2-10 Cable Connectors for Cabled Footswitches. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.14
Figure 2-11 IR Remote Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.16
Figure 2-12 Remote Control Snap Keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.16
Figure 2-13 Battery Orientation in Remote Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.17
Figure 2-14 Change Remote Channel Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.18
Figure 2-15 CENTURION® OZil® Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
Figure 2-16 INFINITI® OZil® Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
Figure 2-17 TurboSonics® Tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.21
Figure 2-18 CENTURION® OZil® Handpiece with Infusion Sleeve. . . . . . . . . . . . . . . . . . . . . . 2.22
Figure 2-19 UltraFlow™* II Handpiece . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.23
Figure 2-20 INTREPID® AutoSert® IOL Injector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.24
Figure 2-21 Vitrectomy Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.26
Figure 2-22 INTREPID® Capsulotomy Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.27
Figure 2-23 Fluidic Management System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.28
Figure 2-24 Standard VideOverlay Front Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.31
Figure 2-25 VideOverlay Rear Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.32
Figure 2-26 Wall Outlet Adapters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.33
Figure 2-27 Standard VideOverlay Connection Diagram. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.33
Figure 2-28 High Definition VideOverlay Connection Diagram. . . . . . . . . . . . . . . . . . . . . . . . . 2.34
Figure 2-29 Navigating the Centurion® Vision System User Screens. . . . . . . . . . . . . . . . . . . . . 2.35
Figure 2-30 Functional Areas of the Setup Screen Using Active Fluidics™ Technology. . . . . . 2.36
Figure 2-31 Drop List of Doctors in System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.37
Figure 2-32 Manage Doctors Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Figure 2-33 Enter Doctor Name Keypad Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Figure 2-34 Manage Doctors Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.39
Figure 2-35 New Doctor Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.39
Figure 2-36 New Doctor Name Added to Drop List of Doctors . . . . . . . . . . . . . . . . . . . . . . . . . 2.39
Figure 2-37 Procedure Type Droplist. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.40
Figure 2-38 Manage Procedures Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.41
Figure 2-39 Procedure Names Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.41
Figure 2-40 Manage Procedures Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.41

viii
FOR REFERENCE ONLY 8065751772
Figure 2-41 Remote Control Snap Navigation Buttons in Continuous Phaco Mode. . . . . . . . . . 2.42
Figure 2-42 Metrics Dialog with Cumulative Dissipated Energy (CDE). . . . . . . . . . . . . . . . . . . 2.44
Figure 2-43 The Setup Status Window. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.46
Figure 2-44 Setup Screen with Custom Drop List Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
Figure 2-45 Doctor Settings Dialog Screen - General Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
Figure 2-46 Doctor Settings Dialog Screen - Fluidics Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.48
Figure 2-47 Doctor Settings Dialog Screen - Footswitch Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.49
Figure 2-48 Doctor Settings Dialog Screen - Sounds Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Figure 2-49 Doctor Settings Dialog Screen - SGS Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Figure 2-50 Doctor Settings Dialog Screen - Advanced Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.51
Figure 2-51 Save As Dialog Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.52
Figure 2-52 System Settings Dialog Screen - General Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53
Figure 2-53 System Settings Dialog Screen - Wireless Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Figure 2-54 Backup/Restore Dialog Screen - Backup Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Figure 2-55 Backup/Restore Dialog Sceren - Restore Tab. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Figure 2-56 Procedure Builder Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.57
Figure 2-57 Procedure Builder Dialog with Available Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.58
Figure 2-58 Procedure Builder Dialog with Fill Step Added. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.58
Figure 2-59 Step Selected in Procedure Builder Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.59
Figure 2-60 Copy (or Rename) Step in Procedure Builder Dialog . . . . . . . . . . . . . . . . . . . . . . . 2.59
Figure 2-61 The About Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Figure 2-62 The Event Viewer Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Figure 2-63 The Shutdown System Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.61
Figure 2-64 The Setup Steps Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62
Figure 2-65 The Centurion® Vision System Surgery Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.64
Figure 2-66 Surgery Control Window with Phaco Surgery Controls Identified. . . . . . . . . . . . . . 2.65
Figure 2-67 Oval Display Button Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.66
Figure 2-68 IP Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.67
Figure 2-69 Fluidics Control Window with Active Fluidics™ Technology Selected . . . . . . . . . 2.69
Figure 2-70 Fluidics Control Window with Gravity Fluidics Selected . . . . . . . . . . . . . . . . . . . . 2.69
Figure 2-71 IOP Setpoints (Fixed) for Active Fluidics™ Technology. . . . . . . . . . . . . . . . . . . . . 2.70
Figure 2-72 IOP Setpoints (Linear) for Active Fluidics™ Technology. . . . . . . . . . . . . . . . . . . . 2.70
Figure 2-73 Surgery Window with Phaco Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Figure 2-74 Surgery Window with I/A Steps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.73
Figure 2-75 Surgery Window with AutoSert® Injector Step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74
Figure 2-76 Surgery Window with Coagulation Step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.74
Figure 2-77 Surgery Window with Anterior Vitrectomy Step. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.75
Figure 2-78 Surgery Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.76
Figure 2-79 Power/Amplitude Dialogs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.78
Figure 2-80 Continuous Phaco Surgery Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.79
Figure 2-81 Footpedal Control in Phaco Modes of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.79
Figure 2-82 Pulse Phaco Surgery Screen and Timing Diagram. . . . . . . . . . . . . . . . . . . . . . . . . . 2.80
Figure 2-83 Burst Phaco Surgery Screen and Timing Diagram. . . . . . . . . . . . . . . . . . . . . . . . . . 2.81
Figure 2-84 The Irrigation/Aspiration Surgery Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.82
Figure 2-85 Footpedal Control in I/A Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.82
Figure 2-86 AutoSert® IOL Injector Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.84
Figure 2-87 Footpedal Control in AutoSert® Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . . . 2.84
Figure 2-88 AutoSert® Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.85

8065751772 ix
FOR REFERENCE ONLY
Figure 2-89 The Coagulation Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.87
Figure 2-90 Footpedal Control in Coagulation Mode of Operation. . . . . . . . . . . . . . . . . . . . . . . 2.87
Figure 2-91 Anterior Vitrectomy Setup Dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.89
Figure 2-92 Footpedal Control in Anterior Vitrectomy Mode of Operation . . . . . . . . . . . . . . . . 2.89
Figure 2-93 Anterior Vitrectomy (Anterior Vit) Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.90
Figure 2-94 Anterior Vitrrectomy (Epi Removal) Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.90
Figure 2-95 Anterior Vitrectomy (I/A Cut) Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91
Figure 2-96 Anterior Vitrectomy (Peripheral Irid) Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91
Figure 2-97 Anterior Vitrectomy (Visco Asp) Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.92

Figure 3-1 U/S Tip/Wrench Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5

Figure 3-2 Phaco Handpiece Tip/Infusion Sleeve Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . 3.6
Figure 3-3 Connect Phaco Handpiece to FMS Tubing and Connector Panel. . . . . . . . . . . . . . . . 3.6
Figure 3-4 Preparing Test Chamber and Placing Handpiece in Pouch. . . . . . . . . . . . . . . . . . . . . 3.6
Figure 3-5 Setting Patient Eye Level (PEL). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.8
Figure 3-6 I/A Handpiece Tip/Infusion Sleeve Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.9
Figure 3-7 Removing Plunger from INTREPID® AutoSert® IOL Injector. . . . . . . . . . . . . . . . . 3.10
Figure 3-8 Vitrectomy Setup Dialog. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.13
Figure 3-9 Preparation of Centurion® UltraVit® Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.14
Figure 3-10 Preparation of Centurion® UltraVit® Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.16

Figure 4-1 Footswitch Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.3

Figure 4-2 Packing System for Transit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.7
Figure 4-3 Setting Up the Reconstitution Rack. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.8

Figure 5-1 Advisories Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.1

Figure 5-2 Warnings Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.2
Figure 5-3 Faults Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.3
Figure 5-4 Troubleshooting Guide. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.4

x
FOR REFERENCE ONLY 8065751772
 LIST OF TABLES

TABLE# TITLE PAGE #

Table 1-1 Guidance and Manufacturer's Declaration - Electromagnetic Emissions. . . . . . . . . . . 1.5
Table 1-2 Guidance and Manufacturer's Declaration - Electromagnetic Immunity . . . . . . . . . . . 1.6
Table 1-3 Recommended Separation Distances Between Portable and Mobile RF
Communications Equipment and the Centurion® Vision System. . . . . . . . . . . . . . . . . 1.7
Table 1-4 Information on Location of Hazardous Substances in Centurion® System. . . . . . . . . 1.10
Table 1-5 Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.24
Table 1-6 Abbreviations Used With the Centurion® Vision System. . . . . . . . . . . . . . . . . . . . . . 1.24
Table 1-7 Summary of Alcon Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.29

Table 2-1 Table of Footpedal Positions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.9

Table 2-2 Footswitch Status LEDs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.13
Table 2-3 Status of Handpiece Ports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.42
Table 2-4 Cumulative Dissipated Energy (CDE). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.44

Table 3-1 Table of Phaco Handpiece Tips and Corresponding Infusion Sleeves . . . . . . . . . . . . . 3.5

Table 4-1 Sterilization Temperature and Time Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.5

Table 5-1 Observed Conditions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.5

Table 5-2 Event Codes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.10

8065751772 xi
FOR REFERENCE ONLY
 PREFACE

This operator's manual is your written guide to the Centurion® Vision System and considers all
options available to the customer; therefore, when reading this manual, ignore the options which do
not apply to your specific unit.

Please read the entire manual carefully before operating the instrument. Recommended settings are
given only as guidelines, and are not meant to restrict the surgeon; however, before trying other
settings, the surgeon and support personnel should be experienced with the system and familiar with
the new settings.

NOTE: If an inconsistency exists between the instructions in the operator's manual and the
Directions For Use (DFU) supplied with a consumable pack or accessory, follow the DFU.

Equipment improvement is an on-going process and, as such, changes may be made to the
equipment after this manual is printed.

Pay close attention to Warnings, Precautions, Cautions, and Notes in this manual. A Warning
statement is written to protect individuals from bodily harm. A Precautionary statement is action
taken in advance to protect against possible danger, failure, or injury; a safeguard. A Caution
statement is written to protect the instrument from damage. A Note is written to bring attention to
highlighted information.

If you have questions, or want additional information, please contact your local Alcon representative
or the Alcon Technical Services Department at:

Alcon Research, Ltd.

15800 Alton Parkway
Irvine, California 92618
(949) 753-1393
FAX (949) 753-6614

CAUTION: U.S. Federal Law restricts this device to sale by or on the order of a physician.

xii
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION ONE
GENERAL INFORMATION

OVERVIEW OF CENTURION® VISION SYSTEM

Alcon’s Centurion® Vision System is an ophthalmic surgical instrument designed to provide

for cataract lens extraction using the CENTURION® OZil® handpiece and the INFINITI®
OZil® handpiece.

The Centurion® Vision System is intended for use in small incision cataract lens extraction
and IOL injection surgical procedures. This system allows the surgeon to emulsify and
aspirate the lens in the eye, while replacing aspirated fluid and lens material with balanced
salt solution. This process maintains a stable (inflated) eye chamber volume. Using system
controls, the surgeon regulates the amount of power applied to the handpiece tip, the rate
of aspiration, vacuum, and the flow of BSS® irrigating solution. The system includes a
footswitch to enable the surgeon to
control flow of fluidics, aspiration
rate, phaco power, vitrectomy cut
rate, IOL injection rate, anterior
capsulotomy, and coagulation
power.

Figure 1-1 The Centurion® Vision System

8065751772 1.1
FOR REFERENCE ONLY
 Key Features of the Centurion® Vision System
• Customized cataract lens removal options:
- High performance CENTURION® OZil® handpiece with ultrasonic torsional
oscillations which can be used exclusively, combined, or alternated with traditional phaco.
- High performance INFINITI® OZil® handpiece with ultrasonic torsional oscillations
which can be used exclusively, combined, or alternated with traditional phaco.
• Advanced fluidics with quick, smooth control of aspiration.
• Advanced Active Fluidics™ technology with quick, smooth control of irrigation flow,
controlled via the front panel, footswitch, or remote control..
• Automated IV pole for traditional gravity fluidics, controlled via the front panel,
footswitch, or remote control.
• Programmable IOP target setting.
• Fully programmable, multi-microprocessor control.
• Modularized fluidic connections with disposable Fluidic Management System (FMS).
• Emulation of venturi-like fluidic performance.
• Power assisted IOL insertion by way of lightweight, autoclavable AutoSert® handpiece.
• Ability to drive a high performance CENTURION® UltraVit® vitrectomy guillotine cutter.
• Bipolar coagulation capability.
• Capsulotomy using the INTREPID® capsulotomy device (ICD, future accessory).
• Several traditional modalities of ultrasonic power control including continuous, pulsed,
and burst application of ultrasonic power, as well as duty cycle management.
• Wireless linear footswitch control of ultrasonic power in phaco steps (sophisticated
control loop offers low-end control).
• Wireless linear footswitch control of aspiration flow rate in I/A, vit, and lens removal
steps.
• Wireless linear footswitch control of vacuum in I/A, vit, and lens removal steps.
• Wireless linear footswitch control of IOL insertion.
• On-demand continuous irrigation.
• Programmable, pressurized reflux via the footswitch.
• Ability to set IOP, vacuum levels, and aspiration flow rates to desired levels in phaco,
I/A, and vit steps.
• Ability to switch between surgical steps using touch screen, remote control, or footswitch.
• Emission of variable tones for confirmation of system operational status.
• Voice confirmation during surgical step or mode changes.
• Articulating flat screen: active matrix color LCD with touch screen.
• High-tech graphical user interface.
• Multi-channel IR remote control.

1.2
FOR REFERENCE ONLY 8065751772
 Indications For Use
The Centurion® Vision System is indicated for emulsification, separation, irrigation, and
aspiration of cataracts, residual cortical material and lens epithelial cells, vitreous aspiration
and cutting associated with anterior vitrectomy, bipolar coagulation, and intra-ocular lens
injection. The AutoSert® IOL Injector Handpiece is intended to deliver qualified AcrySof®
intraocular lenses into the eye following cataract removal.

The AutoSert® IOL Injector Handpiece achieves the functionality of injection of intraocular
lenses. The AutoSert® IOL Injector Handpiece is indicated for use with AcrySof® lenses SN60WF,
SN6AD1, SN6AT3 through SN6AT9, as well as approved AcrySof® lenses that are specifically
indicated for use with this inserter, as indicated in the approved labeling of those lenses.

The Centurion® Vision System, including accessories approved by Alcon, constitutes a complete
surgical system and is intended exclusively for use by licensed ophthalmic surgeons and
their surgical teams. These surgical teams are experienced at conducting phacoemulsification
procedures in a properly maintained surgical environment (qualified personnel, availability of
backup equipment) and are familiar with the operation of the equipment used as outlined in
operator's manuals and directions for use (setup/checkout procedures to be completed before
the surgical procedure; processing of reusable devices; maintenance; etc.).

Patient selection for use with the Centurion® Vision System (such as age, ophthalmic
pathology, and other factors) is determined by the surgeon. The general patient age can range
from newborn to geriatric, although there have been studies that have identified the mean age
of patients that underwent cataract surgery was 72.32 yrs - men and 74.89 yrs - women.1

Intended Use Environments

The Centurion® Vision System is intended for use in hospitals and ambulatory surgery centers.

Phaco Handpiece Note

Throughout the rest of this manual the CENTURION® OZil® handpiece and the INFINITI®
OZil® handpiece will be referred to as phaco handpieces, unless one or the other must be
referred to exclusively.

Trademark Note
A button, mode, or step labeled OZil®, AutoSert®, or UltraChop refers to a display screen
control used with a phaco handpiece, INTREPID® AutoSert® IOL injector, or ALCON®
UltraChopper® tip, respectively.

Abbreviation Descriptions
Many of the abbreviations used in this manual and on the Centurion® Vision System are
described in Table 1-6. Icons are identified in Figure 1-2.

Accessory Equipment
Accessory equipment connected to or used with this equipment must be certified according
to the respective IEC Standard (e.g., IEC 60950-1 for data processing equipment, and IEC
60601-1 for medical equipment). Furthermore, all configurations shall comply with clause 16
of IEC 60601-1:2005 (as amended). Anyone connecting additional equipment or otherwise
1. “Age and sex profile of patients having cataract surgery between 1986 and 2003”
Philip O'Reilly, FRCSI (Ophth), U. Mahmound, FRCOphth, P. Hayes, FRCOphth, P. Tormey, FRCOphth, S. Beatty, MD.
Journal of Cataract Refractive Surgery 2005; 31:2162-2166

8065751772 1.3
FOR REFERENCE ONLY
 causing a different system configuration than provided by Alcon is responsible for continued
compliance to the requirements of clause 16 of IEC 60601-1:2005 (as amended). If in doubt,
consult the Technical Services department or your local Alcon representative.

Follow local governing ordinances and recycling plans regarding disposal or recycling of
device components and packaging.

User Information – Environmental Considerations

The equipment that you have purchased requires the use of natural resources for its
production and operation. This equipment may also contain hazardous substances
which could have potential effect on the environment and human health if disposed of
improperly.

In order to avoid the entry of any such substances into our environment, and to promote
natural resource conservation, please install, maintain, and operate the equipment in
accordance with the instructions. Information on the location of hazardous substances,
resource consumption and emissions of the equipment can be found throughout this
Operator's Manual. Please use the appropriate take-back systems. Such take-back systems
reuse or recycle many of the materials in your end-of-life equipment in a beneficial way.
Please contact your local Alcon office for assistance in take-back options through Alcon
or other providers.

The crossed-bin symbol located on this equipment reminds you to use take-back
systems, while also emphasizing the requirement to collect waste equipment
separately, and not dispose of it as unsorted municipal waste. The Pb notation, if
present, indicates that the labeled device contains greater than 0.004% lead.

If you need more information on the collection, reuse or recycle systems available to
you, please contact your local or regional waste administration, or contact your local
Pb
Alcon office for more information.

Universal Precautions
Universal precautions shall be observed by all people who come in contact with the
instrument and/or accessories to help prevent their exposure to blood-borne pathogens
and/or other potentially infectious materials. In any circumstance, wherein the exact
status of blood or body fluids/tissues encountered are unknown, it shall be uniformly
considered potentially infectious and handled in accordance with OSHA or your own
national guidelines.

EMC Statements
It is important to install and use the equipment in accordance with the instructions in
order to prevent harmful interference with other devices in the vicinity. If this equipment
causes harmful interference to other devices (determined by turning equipment off and
on), the user is encouraged to try to correct interference by one or more of the following
measures:
• Reorient or relocate the other device(s).
• Increase the distance between the equipment.
• Connect this equipment into an outlet on a circuit different from that to which the
other device(s) is connected.
• Consult the manufacturer or your Alcon field service engineer for help.

1.4
FOR REFERENCE ONLY 8065751772
 Users should be aware of known RF sources, such as radio or TV stations and hand-held
or mobile two-way radios, and consider them when installing a medical device or system.

Portable and mobile RF communications equipment such as cellular telephones can affect
medical electrical equipment (see Table 1-3 for recommended separation distances).

Be aware that adding accessories or components, or modifying the medical device or

system, may degrade the EMI performance. Consult with qualified personnel regarding
changes to the system configuration.

WARNINGS!

The use of accessories, transducers, and cables other than those specified, with the
exception of transducers and cables sold by Alcon as replacement parts for internal
components, may result in increased emissions or decreased immunity of the system.

The system should not be used adjacent to, or stacked with, other equipment; and that if
adjacent to or stacked use is necessary, the system should be observed to verify normal
operation in the configuration in which it will be used.

MAGNETIC AND ELECTRICAL INTERFERENCE - Magnetic and electrical fields are

capable of interfering with the proper performance of the device. For this reason make
sure that all external devices operated in the vicinity of the device comply with the
relevant EMC requirements. X-ray equipment, magnetic resonance tomography (MRT),
nuclear magnetic resonance (NMR), or magnetic resonance imaging (MRI) devices are
possible sources of interference as they may emit higher levels of electromagnetic
radiation. See the Magnetic Resonance Unsafe icon in Figure 1-2.

Table 1-1 Guidance and Manufacturer's Declaration - Electromagnetic Emissions - The Centurion®
Vision System is intended for use in the electromagnetic environment specified below. The
customer or the user of the Centurion® Vision System should assure that it is used in such
an environment.

Emissions Test Compliance Electromagnetic Environment-Guidance

RF emissions Group 1 The Centurion® Vision System uses RF energy only for its internal function.
CISPR 11 Therefore, its RF emissions are very low and are not likely to cause any
interference in nearby electronic equipment.

RF emissions Class A The Centurion® Vision System is suitable for use in all establishments
CISPR 11 other than domestic and those directly connected to a low voltage power
supply network that supplies buildings used for domestic purposes.
Harmonic emissions Class A
IEC 61000-3-2 The EMC Statement provides guidance on steps to take in case of
electromagnetic interference.
Voltage fluctuations/ Complies
Flicker emissions
IEC 61000-3-3

8065751772 1.5
FOR REFERENCE ONLY
Table 1-2 Guidance and Manufacturer's Declaration - Electromagnetic Immunity - The Centurion® Vision
System is intended for use in the electromagnetic environment specified below. The customer or
the user of the Centurion® Vision System should assure that it is used in such an environment.

Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment-Guidance

Electrostatic discharge • ±6 kV contact • ±6 kV contact Floors should be wood, concrete, or ceramic tile. If floors
(ESD) • ±8 kV air • ±8 kV air are covered with synthetic material, the relative humidity
IEC 61000-4-2 should be at least 30 %.

Electrical fast • ±2 kV for power supply • ±2 kV for power supply Mains power quality should be that of a typical hospital
transient/burst lines lines (including ambulatory surgery center) environment. To avoid
IEC 61000-4-4 • ±1 kV for input/output • ±1 kV for input/output pre-mature shutdown due to fast transients avoid powering
lines lines the Centurion® Vision System on the same branch circuit
with sources that can generate fast transients (inductive
switching; e.g., high current motors).

Surge • ±1 kV differential mode • ±1 kV differential mode Mains power quality should be that of a typical hospital
IEC 61000-4-5 • ±2 kV common mode • ±2 kV common mode (including ambulatory surgery center) environment.

Voltage dips, short • < 5 % UT (> 95 % dip in • < 5 % UT (> 95 % dip in Mains power quality should be that of a typical hospital
interruptions, and UT) for 0.5 cycle UT) for 0.5 cycle (including ambulatory surgery center) environment.
voltage variations on • 40 % UT (60 % dip in • 40 % UT (60 % dip in If the use of the Centurion® Vision System requires
power supply input UT) for 5 cycles UT) for 5 cycles continued operation during power mains interruptions,
lines • 70 % UT (30 % dip in • 70 % UT (30 % dip in it is recommended that the Centurion® Vision System
IEC 61000-4-11 UT) for 25 cycles UT) for 25 cycles be powered from an uninterruptible power supply with a
• < 5 % UT (> 95 % dip in • < 5 % UT (> 95 % dip in minimum rating of 1200VA.
UT) for 5 s UT) for 5 s

Power frequency 3 A/m 3 A/m Power frequency magnetic fields should be at levels
(50/60 Hz) characteristic of a typical location in a typical hospital
magnetic field (including ambulatory surgery center) environment.
IEC 61000-4-8

Portable and mobile RF communications equipment should

be used no closer to any part of the Centurion® Vision
System, including cables, than the recommended separation
distance calculated from the equation applicable to the
frequency to the transmitter.

Recommended separation distance:

Conducted RF 3 Vrms 3 Vrms d = 1.2√P

IEC 61000-4-6 150 kHz to 80 MHz

Radiated RF 3 V/m 3 V/m d = 1.2 √ P 80 MHz to 800 MHz

IEC 61000-4-3 80 MHz to 2.5 GHz
d = 2.3 √ P 800 MHz to 2.5 GHz

where P is the maximum output power rating to the

transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).

Field strength from fixed RF transmitters, as determined

by an electromagnetic site surveya, should be less than
the compliance level in each frequency rangeb.

Interference may occur in the vicinity of

equipment marked with following symbol.

Note: UT is the a.c. mains voltage prior to application of the test level.
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects, and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) and land mobile radios, amateur radio, AM and
FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To access the electromagnetic environment due
to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the
(equipment or system) is used exceeds the applicable RF compliance level above, the (equipment or system) should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating
the Centurion® Vision System.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

1.6
FOR REFERENCE ONLY 8065751772
Table 1-3 Recommended Separation Distances Between Portable and Mobile RF Communications
Equipment and the Centurion® Vision System - The Centurion® Vision System is intended
for use in an electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the Centurion® Vision System can help prevent electromagnetic
interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the Centurion® Vision System as recommended
below, according to the maximum output power of the communications equipment.

Separation distance according to frequency of transmitter

Rated maximum output (m)
power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
(W) d = 1.2 √ P d = 1.2 √ P d = 2.3 √ P

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23

For transmitters rates at a maximum output power not listed above, the recommended separation distance d in meters (m) can
be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
Note 1 - At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2 - These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects, and people.

8065751772 1.7
FOR REFERENCE ONLY
 Equipment Contains Radio Transmitters

The Centurion® Vision System is a medical device designed for Indoor Use Only, that
incorporates short-range frequency radio transmitters for use solely by the Centurion®
system for communication with system components. These short-range frequency radio
transmitters meet the EU and AFTA countries requirements. They are also FCC; IC;
R&TTE 1999/5/EC and Japanese Radio Law compliant.

• ZigBee Radio Modular (Communication link with Footswitch, SGS and Media Center)
- Frequency or frequency band of transmission: 2.405 – 2.480 GHz
- Type and frequency characteristics of the modulation: OQPSK (Offset quadrature
phase-shift keying)
- The Effective Radiated Power (ERP): 12.91 dBm (19.54 mW)

• Wireless LAN device (Optional)

- Frequency or frequency band of transmission: 2.412 – 2.484 GHz and 5.180 - 5.700 GHz
- Type and frequency characteristics of the modulation: OFDM, DSSS, CCK, DQPSK,
DBPSK, 64 QAM, 16 QAM
- The Effective Radiated Power (ERP): 17.09 dBm (51.17 mW)

• Wireless Footswitch Charger

- Frequency or frequency band of charging transmission: 50 kHz
- Frequency or frequency band communication transmission: 115 kHz
- Type and frequency characteristics of the modulation: FSK (Frequency Shift Keying)
- The Effective Radiated Power (ERP): -14.89 dBm (53.18 μW)

USA – Federal Communications Commission (FCC)

This device complies with part 15 of the FCC Rules. Operation is subject to the following
two conditions: (1) This device may not cause harmful interference, and (2) this device
must accept any interference received, including interference that may cause undesired
operation.

CAUTION
Change or modifications made to this equipment (including antenna) not expressly
approved by Alcon may void the FCC authorization to operate this equipment.

FCC Radiation Exposure Statement

CAUTION
To ensure that the radio transmitter complies with current FCC regulations limiting
both maximum output RF power and human exposure to radio frequency radiation, a
separate distance of at least 20 cm must be maintained between the unit’s antenna and
the body of the user and any nearby persons at all times, and unit’s antenna must not
be co-located or operating in conjunction with any other antenna or transmitter.

1.8
FOR REFERENCE ONLY 8065751772
 Canada – Industry of Canada (IC)
This device complies with Industry Canada licence-exempt RSS standards. Operation
is subject to the following two conditions: (1) This device may not cause harmful
interference, and (2) this device must accept any interference, including interference that
may cause undesired operation of the device.

Cet appareil est conforme aux normes d’Industrie Canada RSS exemptes de licence.
Son fonctionnement est soumis aux deux conditions suivantes: (1) Cet appareil ne
doit pas provoquer d’interférences nuisibles, et (2) cet appareil doit accepter toute
interférence, y compris les interférences pouvant provoquer un fonctionnement
indésirable de l’appareil.

Transmitter Antenna:
Under Industry Canada regulations, this radio transmitter may only operate using an
antenna of a type and maximum (or lesser) gain approved for the transmitter by Industry
Canada. To reduce potential radio interference to other users, the antenna type and its
gain should be so chosen that the equivalent isotropically radiated power (e.i.r.p.) is not
more than that necessary for successful communication.

Conformément à la réglementation de l’industrie du Canada, cet émetteur de radio

ne peut être utilisé qu’avec un type d’antenne approuvé pour l’émetteur par Industrie
Canada et seulement avec une valeur de gain inferieur ou égale au gain maximum
approuvé par Industrie Canada. Pour réduire les risques potentiels d’interférence
à autrui, le type d’antenne et son gain doivent être choisis de sorte que la puissance
isotrope rayonnée équivalente (p.i.r.e.) ne dépasse pas la valeur qui est nécessaire
pour une communication réussi.

Exposure of Humans to RF Fields:

This device complies with the RF exposure limits for humans as called out in RSS-102.

Cet appareil est conforme aux limites d’exposition RF pour les êtres humains comme
elles le sont notifiées dans la norme RSS-102.

8065751772 1.9
FOR REFERENCE ONLY
 Europe – R&TTE Directive 99/5/EC

This device complies with the requirements of the Council Directive 99/5/EC (R&TTE).

CAUTION
The radio equipment is intended to be used in all EU and AFTA countries. Outdoor
use may be restricted to certain frequencies and/or may require a license for
operation. Contact local Authority for procedure to follow.

PRECAUTION: Combinations of power levels and antennas resulting in a radiated

power of above 100 mW equivalent isotropic radiated power (e.i.r.p) are considered as
not compliant with the above mentioned directive and are not allowed for use within the
European community and countries that have adopted the European R&TTE directive
1999/5/EC.

For more details on legal combinations of power levels and antennas, contact Alcon
Compliance.

Japan

This device complies with Japanese Radio Law.

Table 1-4 Information on the Location of Hazardous Substances in the Centurion® Vision System -
The Centurion® Vision System contains hazardous substances which could have potential
effect on the environment and human health if disposed of improperly.

Material Location Hazardous Substances Contained

Printed Circuit Board Assembly Lead, Polybrominated Biphenyls (PBB)
Other Electrical / Electronic Device Lead, Polybrominated Biphenyls (PBB)
Cable Assembly Lead
Power Supply Lead, Polybrominated Biphenyls (PBB)
Host PC Module Lead, Polybrominated Biphenyls (PBB)
Liquid Crystal Display Lead
Battery Lead, Lithium, Zn/MnO2
IV Pole Assembly Lead, Polybrominated Biphenyls (PBB)
Remote Control Lead
Fluidics Assembly Lead
Pneumatic Assembly Lead

1.10
FOR REFERENCE ONLY 8065751772
WARNINGS AND CAUTIONS

Many of these warnings are stated elsewhere in this manual; however, for easy reference
they are repeated in greater detail here. If additional information is required, please
contact your local Alcon service representative, or the Technical Services Department.

There are no user serviceable components inside the Centurion® Vision System console
or footswitch. Refer all service issues to your factory-trained Alcon service engineer.

WARNINGS!
To avoid risk of electric shock, this equipment must only be connected to a supply
mains with protective earth (ground).

The Centurion® Vision System battery can only be serviced by a factory-trained Alcon
service engineer. Access by untrained personnel can lead to injury.

A qualified technician must perform a visual inspection of the following components

every twelve months:
• Warning Labels (see Figure 1-3)
• Power Cord
• Fuses
In case of a deficiency, do not use the system; call Alcon Technical Services.

A qualified technician must check ground continuity and leakage current every twelve
months to ensure they are within the limits of the applicable standards (for example:
EN60601-1/IEC60601-1). Values must be recorded, and if they are above the limits of
the applicable standards, or 50 % above initial measurement, do not use the system;
call Alcon Technical Services.

If the Centurion® Vision System is used at the 220 V - 240 V range in the United States
or Canada, it should be used on a center-tapped, 240 V single phase circuit.

Console isolation from mains is achieved through a two pole power switch. Turn OFF
power switch or unplug the power cord from wall outlet to achieve isolation from mains.

Do not use the Centurion® Vision System near flammable anesthetics.

Do not exceed maximum capacity of drain bag (500 ml). Excessive pressure can result
from exceeding drain bag maximum capacity and potentially result in a hazardous
condition for the patient.

Inadvertent actuation of Prime or Tune while a handpiece is in the eye can create a
hazardous condition that may result in patient injury.

Keep clear of display base when raising display from stored position to prevent skin,
hair, and /or clothing from being trapped at the base.

The maximum allowable load on the instrument tray is 20 lb. (9 kg).

Place the instrument tray in the stored position prior to transportation to avoid a
situation that could cause the system to tip.

Console might overbalance when it is pushed and its wheels are immobilized (blocked).

Route the footswitch cable, power cord and any other cables connected to the
Centurion® Vision System to avoid tripping.

8065751772 1.11
FOR REFERENCE ONLY
 WARNINGS!
Appropriate use of Centurion® Vision System parameters and accessories is
important for successful procedures. Use of low vacuum limits, low flow rates, low
bottle heights, high power settings, extended power usage, power usage during
occlusion conditions (beeping tones), failure to sufficiently aspirate viscoelastic
prior to using power, excessively tight incisions, and combinations of the above
actions may result in significant temperature increases at incision site and inside
the eye, and lead to severe thermal eye tissue damage.

Good clinical practice dictates testing for adequate irrigation, aspiration flow, reflux,
and operation as applicable for each handpiece prior to entering eye.

Ensure that the tubings are not occluded during any phase of operation.

If the handpiece test chamber is collapsed after tuning, there is a potential of low
irrigation flow through the handpiece and may result in a fluidic imbalance. This, in
turn, may cause a shallowing or collapsing of the anterior chamber.

Avoid setting the patient above the FMS unless PEL is used. Operating with the patient
above the FMS without PEL adjustment will result in a lower irrigation pressure than
indicated on the display, and possible underventing.

Use of BSS® irrigating fluid bags other than those approved by Alcon for use in the
Active Fluidics™ system can result in patient injury or system damage.

Use of appropriate technique and settings is important to minimize fragments and

turbulence.

Do not remove the FMS during the surgical procedure.

In the event of a system error release footswitch to the up position.

Improper handling or removal of dual irrigation handpiece tip from eye may cause
draining of the fluidics system.

CAUTIONS
• Modification of the equipment is NOT allowed without prior authorization
from the manufacturer. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe use of the equipment.
• Avoid spilling BSS® irrigating solution, or moisture of any kind, around the
electrical handpiece connectors.
• Do not spray any liquid (i.e. cleaning solution or water) upward into the
console vents.
• Do not push or pull the unit by the display, the instrument tray, or the IV pole.
Wrapping around the rear and sides of the system is a handle provided for
moving the instrument. The unit should be pulled and not pushed, especially
over elevator and door thresholds.

1.12
FOR REFERENCE ONLY 8065751772
 Phaco Handpiece Care

Phaco handpieces are surgical instruments and must be handled with care. The
handpiece tip should not touch any solid object while in operation. Immediately
following surgery the handpiece must be thoroughly cleaned. Be sure handpiece
connector is completely dry before connecting it to console. For cleaning and
sterilization procedures, see the Directions for Use (DFU) supplied with the
handpiece.

WARNINGS!

If in the medical opinion of the physician a patient with a prion related disease
undergoes a high risk procedure, the instrument should be destroyed or be processed
according to local requirements.

Use of a phaco handpiece in the absence of irrigation flow and/or in the presence of
reduced or lost aspiration flow and/or sideways orientation of the Kelman® and OZil® 12
tips can cause excessive heating and potential thermal injury to adjacent eye tissues.

Appropriate use of Centurion® Vision System parameters and accessories is important

for successful procedures. Use of low vacuum limits, low flow rates, low bottle
heights, high power settings, extended power usage, power usage during occlusion
conditions (beeping tones), failure to sufficiently aspirate viscoelastic prior to using
power, excessively tight incisions, and combinations of the above actions may result
in significant temperature increases at incision site and inside the eye, and lead to
severe thermal eye tissue damage.

Use of an ultrasonic handpiece other than an OZil® torsional handpiece, or use of a

handpiece repaired without Alcon authorization, is not permitted, and may result in
patient injury, including potential shock hazard to patient and/or operator.

The U/S tips supplied in the Centurion® Vision System pack are only to be used on
an OZil® torsional handpiece. Each U/S tip is intended to be used only once per case,
and then disposed of according to local governing ordinances.

Mismatching U/S tips and infusion sleeves may create potentially hazardous fluidic
imbalances.

Directing energy toward non-lens material, such as iris or capsule, may cause
mechanical and/or thermal tissue damage.

Perform visual inspection of accessories for burs or bent tips prior to use.

Use of appropriate technique and settings is important to minimize fragments and

turbulence.

8065751772 1.13
FOR REFERENCE ONLY
 CAUTIONS

Never ultrasonically clean the phaco handpiece; irreparable damage may result.

Prior to sterilization, the phaco handpiece should always have the connector end
cap secured and placed in the sterilization tray. This will prevent damage to the
connectors and handpieces during handling, and especially during autoclaving.

The phaco handpiece and INTREPID® AutoSert® IOL Injector must be at room
temperature just before use. Allow the handpiece to air cool for at least 15
minutes after autoclaving; never immerse the handpiece in liquid when hot.

Do not operate the phaco handpiece unless the tip is immersed in BSS® sterile
irrigating solution or distilled water or is in surgical use. Irreparable damage to
the handpiece and tip can result if run dry.

Ensure that test chamber is filled with BSS® sterile irrigating solution before
tuning the phaco handpiece. Tuning a handpiece dry may result in premature tip
failure and breakage.

Quenching a hot handpiece in water can cause damage and will void warranty.

Be sure handpiece is completely dry before connecting it to console. Damage to

handpiece and console may result if plugged in when wet.

Phaco Handpiece Tips

Ensure that handpiece tip is fully tightened to the handpiece. If not securely attached,
an error may be generated and/or inadequate tuning will occur. Ensure that the tip is
not too tight so that it can be removed after use.

Use of a tool other than tip wrenches supplied by Alcon may cause damage to the tip
and/or handpiece.

WARNING!
Poor clinical performance will result if tip is not secured tightly to the handpiece.

During any ultrasonic procedure, metal particles may result from inadvertent
touching of the ultrasonic tip with a second instrument. Another potential source
of metal particles resulting from any ultrasonic handpiece may be the result of
ultrasonic energy causing micro abrasion of the ultrasonic tip.

1.14
FOR REFERENCE ONLY 8065751772
 Ultraflow™* II I/A Handpiece

Prior to each procedure inspect the two O-rings where the tip screws onto the
Ultraflow™* II I/A handpiece. If damaged or missing, replace the o-rings. If in doubt,
contact Alcon's Technical Services Department.

WARNINGS!
Use of non-Alcon surgical reusable or disposable I/A handpieces that do not meet
Alcon surgical specifications, or use of an Alcon handpiece not specified for use with
the Centurion® Vision System, may result in a fluidic imbalance. This, in turn, may
cause a shallowing or collapsing of the anterior chamber.

Exceeding the recommended level of 100 mmHg (133 hPa) with a 0.5 mm or larger
I/A tip may cause anterior chamber shallowing and/or incarceration or tearing of
posterior capsule.

I/A tips are not to be used with a phaco handpiece.

Recommended Vacuum Range for I/A Tips

It is important that only the proper size I/A tip be used when operating with maximum
vacuum. Only 0.2 mm or 0.3 mm I/A tips should be used with vacuum limits above
100 mmHg (133 hPa). I/A adjustable vacuum range is 0 - 700 mmHg (0 - 933 hPa).

Centurion® Vitrectomy Probe

The vitrectomy probe, a guillotine vitreous cutter, is intended for single use only.

Vitrectomy cutting performance may vary at high altitudes. Consult Alcon Technical
Service for additional information.

WARNINGS!
Do not test or operate vitrectomy probe unless tip of probe is immersed in BSS ®
sterile irrigating solution or distilled water or is in surgical use. Irreparable
damage to the probe and tip can result if run dry.

Perform visual inspection of accessories for burs or bent tips prior to use.

Connect pneumatic tubing connectors from vitrectomy probe to console prior to

initiating prime of probe. Initiating prime of the vitrectomy probe, or running the
vitrectomy system, with one or both pneumatic connectors disconnected may cause
the flow of non-sterile air over the sterile field for a brief moment.

Do not use vitrectomy probes that are not approved for use on Centurion® system.

After filling and testing, and before surgical use, verify that the probe is properly
actuating and aspirating. This may require lowering cut rate to achieve good
visualization. The port should always remain in open position in footpedal position 1.
If cutting port is partially closed while in position 1, replace the probe. Prior to entry
into the eye, and with tip of probe in sterile irrigating solution, the surgeon
should step on the footpedal for visual verification that the probe is cutting:
• If the cutter is observed to not fully close, or does not move when the probe
is actuated, replace the probe.
• If cutting port is partially closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the probe tip during
priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during the surgical
procedure, stop immediately and replace the probe.

8065751772 1.15
FOR REFERENCE ONLY
 INTREPID® AutoSert® IOL Injector

CAUTIONS
• Do not ultrasonically clean the AutoSert® IOL Injector connector. Ultrasonic
cleaning will cause irreparable damage.
• Use care when handling AutoSert® IOL Injector, particularly when cleaning. Always
clean handpiece over a surface cushioned with a pad or rubber mat.
• Be sure handpiece cable connector is dry before connecting it to the console.
• Do not disconnect cable connector from Centurion® system console until the IOL
Injector plunger is fully retracted.
• Do not immerse the AutoSert® IOL Injector in any fluid when the plunger is not
retracted.
• As part of a properly maintained surgical environment, it is recommended that
a backup IOL injector be made available in the event the AutoSert® IOL injector
handpiece does not perform as expected.

WARNINGS!
• The INTREPID® AutoSert® IOL Injector is non-sterile and must be cleaned and
sterilized prior to, and immediately after, each use.
• Never immerse the IOL injector in liquid after autoclaving; allow it to air cool for at
least 15 minutes. Quenching could result in a potentially hazardous condition for
the patient.
• The AutoSert® IOL Injector delivery system is for the implantation of Alcon qualified
AcrySof® foldable IOLs. Unqualified lenses shall not be used with the system. See
INTREPID® AutoSert® IOL Injector DFU or AcrySof® IOL DFU, or contact your Alcon
representative, for qualified lens/cartridge combinations.
• The cartridge/IOL combination listed in the DFU, along with Alcon settings, has
been validated per section 5 of BS EN ISO 11979-3:2006. Appropriate use of injector
handpiece settings is important for successful IOL implantation. Inappropriate use
of settings may lead to a potentially hazardous condition for the patient.
• Fully retract plunger before detaching nosecone from AutoSert® IOL Injector;
otherwise, this could expose non-sterile portion of shaft and result in a potentially
hazardous condition for the patient.
• For the intended IOL to be implanted, the proper Cartridge profile must be selected
from the driving console, and the proper plunger must be attached to the AutoSert®
IOL Injector. Failure to do so can result in a potentially hazardous condition for patient.
• The metal reusable plunger must be sterilized after each use. The reusable plunger
is to be installed onto the handpiece or into the wrench prior to sterilization.

Aspiration/Vacuum Adjustments

Adjusting aspiration rates or vacuum limits above the preset values may result in
aspiration levels (volumes) exceeding irrigation inflow.

WARNING!
Adjusting aspiration rates or vacuum limits above the preset values, or lowering the
IOP or IV pole below the preset values, may cause chamber shallowing or collapse
which may result in patient injury.

1.16
FOR REFERENCE ONLY 8065751772
 Presurgical Check-out Tests

Presurgical check-out tests must be performed as outlined in Section Three of this

manual (Operating Instructions). If an Event message is displayed on the front panel,
refer to the Troubleshooting section of this manual. If the problem persists, DO NOT
PROCEED.

WARNINGS!
When filling handpiece test chamber, if stream of fluid is weak or absent, good
fluidics response will be jeopardized. Good clinical practice dictates the testing for
adequate irrigation and aspiration flow prior to entering the eye.

Ensure that tubings are not occluded or pinched during any phase of operation.

Perform visual inspection of accessories for burrs or bent tips prior to use.

IV Pole

WARNINGS!

Keep clear of the IV pole when it is in motion to prevent skin, hair, and/or clothing
from being trapped in the IV pole mechanism. The IV pole moves during power on/
off, priming, and bottle height adjustment.

IV pole rises automatically. To avoid stretching drip chamber tubing, and possibly
pulling drip chamber out of bottle, tubing must hang freely with no interference.

When out of use, remove fluid bottle from IV pole and flip bottle hanger into its storage
position to avoid injury.

Empirical numbers for bottle heights are not a replacement for competent surgical
technique. The surgeon should visually and physically monitor intraocular pressure.

Footswitch

If required, the footswitch may be wiped with alcohol, mild soap and water, or any
germicidal solution that is compatible with the plastic parts.

WARNING!
Route the footswitch cable properly to avoid tripping.

CAUTIONS
Do not clean the footswitch using solvents, abrasives, or any cleaner that is not
compatible with plastic parts made of LEXAN EXL9112. Damage may result.

Never pick up or move the footswitch by the cable. Dropping or kicking the
footswitch can cause irreparable damage.

8065751772 1.17
FOR REFERENCE ONLY
 Occlusion Tones

Two different occlusion tones (intermittent beeping tones during occlusion) indicate
that the vacuum is near or at its preset limit, and aspiration flow is reduced or stopped
to avoid exceeding the limit. The first type, the I/A occlusion tone, sounds when
occlusion occurs during aspiration only (in the absence of ultrasonic power). The
I/A occlusion tone is a lower, intermittent single beep. The second type of occlusion
tone, the phaco occlusion tone, is a higher, intermittent double beep, and sounds when
occlusion occurs during application of ultrasonic power.

The I/A occlusion and phaco occlusion tones indicate that the vacuum has reached its
maximum allowed preset value. The I/A occlusion tone can be turned off, while the
phaco occlusion tone cannot be turned off.

WARNINGS!
The phaco occlusion bell indicates no aspiration flow. Use of high phaco settings
and/or prolonged use may lead to thermal injury.

Use of the phaco handpiece in the absence of irrigation flow and/or in the presence
of reduced or lost aspiration flow can cause excessive heating and potential thermal
injury to adjacent eye tissues.

In the event of a persistent loss of aspiration during the application of phaco

power, remove phaco power via footswitch control.

Vacuum Tone

A vacuum tone is provided. The pitch will vary relative to the amount of vacuum. A
high vacuum can indicate that little to no flow is occuring. This tone can be reduced
in volume, but not turned off.

WARNINGS!
A moderate to high vacuum tone may indicate little to no flow is occuring. Use of the
phaco handpiece in the absence of irrigation flow and/or in the presence of reduced
or lost aspiration flow can cause excessive heating and potential thermal injury to
adjacent eye tissues.

Do not exceed maximum capacity of drain bag (500 ml). Excessive pressure in drain
bag can result from exceeding its maximum capacity and potentially result in a
hazardous condition for the patient.

In the event of a persistent loss of aspiration during the application of phaco

power, remove phaco power via footswitch control.

Cautery, Diathermy, Coagulation Definition

The Centurion® Vision System uses the word “Coagulation” in place of Cautery or
Diathermy, based on the following definition:

Coagulation - Isolated, bipolar, high frequency current supplied to conductors (e.g.

forceps). Current passes between these electrodes, halting bleeding. (Abbreviated
“Coag” in some of the text of this operator’s manual.)

1.18
FOR REFERENCE ONLY 8065751772
 Coagulation Function

Listed below are general precautions to be followed when using the Coagulation function:

• To ensure safe operation of the coagulation function, only approved cables

and accessories must be used (See your Alcon representative). Coagulation
performance can be guaranteed only when using Alcon components or Alcon-
endorsed components.
• To reduce the risk of accidental burns, caution should always be taken when
operating high-frequency surgical equipment.
• Interference produced by the operation of high-frequency surgical equipment may
adversely influence the operation of other electronic equipment.
• Accessories should be checked regularly; electrode cables should particularly be
checked for possible damage to the insulation.
• Operation of the coagulation step is limited to extraocular uses only.
• The lowest power level in coagulation step should always be selected for the
intended purpose.
• Skin-to-skin contact (for example between the arms and body of the patient)
should be avoided, for example by insertion of dry gauze.
• When HF (high frequency) surgical equipment and physiological monitoring
equipment are used simultaneously on the same patient, any monitoring electrodes
should be placed as far as possible from the surgical electrodes. Needle monitoring
electrodes are not recommended.
• In all cases, monitoring systems incorporating high frequency current-limiting
devices are recommended.
• The cables to the surgical electrodes should be positioned in such a way that
contact with the patient or other leads is avoided.
• Temporarily unused active electrodes should be stored so that they are isolated
from the patient.
• The use of flammable anaesthetics or oxidizing gases such as nitrous oxide (N2O)
and oxygen should be avoided if a surgical procedure is carried out in the region of
the thorax or the head, unless these agents are sucked away.
• Non-flammable agents should be used for cleaning and disinfection wherever possible.
• Flammable agents used for cleaning or disinfecting, or as solvents of adhesives,
should be allowed to evaporate before the application of HF surgery. Some
materials, for example cotton, wool and gauze, when saturated with oxygen may
be ignited by sparks produced in normal use of the HF surgical equipment.
• Accessories should have a rated voltage equal to or greater than the maximum
coagulation output voltage.

WARNINGS!
Do not use the coagulation function on patients with pacemakers or implanted
defibrillatory devices. If electrosurgery is used on patients with implanted cardiac
pacemakers or defibrillatory devices or pacemaker electrodes, be aware that
irreparable damage to the pacemaker or defibrillatory device and its function
may occur and lead to ventricular fibrillation. Please check with the pacemaker
or defibrillatory device manufacturers for their recommendations.

Failure of the HF surgical equipment (coagulation circuitry) could result in an

unintended increase of output power.

8065751772 1.19
FOR REFERENCE ONLY
 VideOverlay System

WARNINGS!
Do not remove VideOverlay cover; there are no user-serviceable parts inside.
Refer servicing to qualified service personnel.

Do not simultaneously touch the VideOverlay enclosure and the patient.

CAUTIONS
• Do not use multiple portable socket outlets with this system.
• Use only the Alcon-supplied serial cable to connect the Centurion® Vision
System to the VideOverlay System.

1.20
FOR REFERENCE ONLY 8065751772
 Consumable Packs

Consumable items used with the Centurion® Vision System during surgery are
designed to be used once and then discarded, unless labeled otherwise.

All Centurion® packs contain Directions for Use (DFU). It is important to read and
understand the DFU’s prior to use.

In all cases, the instrument setup instructions contained in the manual should be
thoroughly understood prior to using any of the pack configurations.

PRECAUTION: If an inconsistency exists between the instructions in the operator’s

manual and the Directions For Use (DFU) supplied with a consumable pack or
accessory, follow the DFU.

WARNINGS!

Mismatch of consumable components and use of settings not specially adjusted for
a particular combination of consumable components may create a patient hazard.

Do not use packs that have exceeded the expiration date.

Sterile disposable medical devices should not be reused! These components have
been designed for one time use only; do not reuse.

Potential risk from reuse or reprocessing the following products labeled for single
use include:
• Bipolar Coagulation Instruments - Thermal injury or electrical shock caused by a
damaged bipolar instrument, and foreign particle introduction into the eye.
• Fluid Management Components - Fluid path leaks or obstruction resulting in reduced
fluidics performance, and foreign particle introduction into the eye.
• Phacoemulsification Tips - Reduced tip cutting performance, presence of tip burrs,
fluid path obstruction, and foreign particle introduction into the eye.
• Vitreous Cutting Instruments - Reduced vitreous cutting performance, fluid path
obstruction, and foreign particle introduction into the eye.

The equipment used in conjunction with the Alcon disposables constitutes a complete
surgical system. Use of disposables other than Alcon disposables may affect system
performance and create potential hazards, and if it is determined to have contributed
to the malfunction of the equipment under contract, could result in the voidance of
the contract and/or invoicing at prevailing hourly rates.

Perform visual inspection of accessories for burs or bent tips prior to use.

Do not remove the FMS during the procedure.

Do not use any Vitrectomy probes that have not been approved for use on the
Centurion® Vision System.

8065751772 1.21
FOR REFERENCE ONLY
PRODUCT SERVICE

For product service, please contact Alcon’s Technical Services Department at the
number provided below.

Operators experiencing problems with the system should refer to the Operating
Instructions and Troubleshooting sections of this manual. A problem which persists
should be referred to the Alcon Technical Services Department or your local
authorized service representative.

For optimum performance, it is the user’s responsibility to schedule preventive

maintenance service on the system and its accessories a minimum of one time per
year. Additional preventive maintenance may be required based upon system use.
Alcon’s Field Service Engineers are trained and equipped to provide the highest
quality of workmanship.

Safety performance should be verified by the user (e.g., qualified service personnel) at
least twice a year. Ground resistance, leakage current, and dielectric withstand voltage
must be checked to appropriate national standard.

To avoid unnecessary shipping, please contact your Alcon Technical Services

Department prior to return of any system or accessories. If return of the equipment is
deemed necessary, a Return Material Authorization will be issued with appropriate
shipping instructions.

Alcon Technical Services Department

15800 Alton Parkway
Irvine, California 92618-3818
(800) 832-7827, or (949) 753-1393

1.22
FOR REFERENCE ONLY 8065751772
LIMITED WARRANTY

Alcon will repair or replace at its option, any system or accompanying accessories
found to be defective in material and/or workmanship for a period of one (1) year
from the date of initial installation. This warranty applies to the original purchaser
of the system, when said system is properly installed, maintained, and operated in
accordance with published instructions.

Alcon shall not be obligated to provide services under this warranty for damage to
or destruction of systems covered where such damage or destruction is a result of
or caused by fire or explosion of any origin, riot, civil commotion, aircraft, war, or
any Act of God including, but not limited to lightning, windstorm, hail, flood or an
earthquake.

This warranty does not cover damage resulting from service repair or other alteration
by any person other than an Alcon-authorized service person, and any warranties
provided by Alcon with respect to this equipment shall become void and of no further
force and effect if this equipment is serviced by anyone other than Alcon-authorized
service personnel. In particular, Alcon shall have no obligation to replace, repair or
credit customer’s account for the cost of the equipment, which has been subject to
service or other alteration by persons other than Alcon-authorized service personnel.

The express warranty above is the sole warranty obligation of Alcon, and the
remedy provided above is in lieu of any and all other remedies. There are no other
agreements, guarantees, or warranties – oral or written, expressed or implied –
including , without limitation, warranties of merchantability or fitness for a particular
purpose. Alcon shall have no liability whatsoever for any incidental or consequential
damages arising out of any defect, improper use, or unauthorized service or repair.

WARNING!
The consumable products used in conjunction with ALCON® instrument
products constitute a complete surgical system. Use of consumable products
and handpieces other than those manufactured by Alcon may affect system
performance and create potential hazards. If it is determined that consumable
products or handpieces not manufactured by Alcon have contributed to the
malfunction of the equipment during warranty period, service will be provided
at prevailing hourly rates.

8065751772 1.23
FOR REFERENCE ONLY
 Product Requirements Performance Requirements

Console Dimensions: Phacoemulsification:

Height: No greater than 165 cm (65 in) (CENTURION® OZil® handpiece and INFINITI® OZil® handpiece)
Width: No greater than 58.5 cm (23 in) Submodes: Continuous, Burst, Pulse
Depth: No greater than 76 cm (30 in) Longitudinal Tip Stroke @ 100 %: .0084 ± .0018 cm (.0033 ± .007 in)
Console Weight: Resonant Frequency: 30 kHz to 60 kHz
Unpackaged: No greater than 107 kg (235 lb) Torsional Tip Stroke @ 100 %: .0069 ± .0023 cm (.0027 ± .0009 in)
Packaged: No greater than 150 kg (330 lb) Resonant Frequency: 30 kHz to 60 kHz
Environmental Limitations – Operating: Pulse Rate Range: 1 - 250 pps
Altitude: 3,000 m (9,842 ft) On Time: 0 - 100 %
Temperature: 10 °C to 35 °C (50 °F to 95 °F) Burst On Time: 2 - 500 ms
Relative Humidity: 10 % to 95 % without condensation Burst Off Time: 2500 - 0 ms
Environmental Limitations – Non-Operating: Anterior Vitrectomy:
Altitude: 5600 m (18,300 ft) Submodes: Anterior Vit, Epi Removal, I/A Cut, Peripheral Irid, Visco-Asp
Temperature: -40 °C to 70 °C (-40 °F to 158 °F) CENTURION® UltraVit® Probe: 1 to 4,000 cpm
Relative Humidity: 10 % to 95 % without condensation Diathermy (Coagulation):
Shock, Bump & Drop: 10 W max, 75 Ω load
The system conforms to EN ISO 15004-1 requirements for vibration, bump, 76 Vpp @ 1.5 MHz ± 5 %, 75 Ω load
and shock. Waveshape: Sinusoidal
Caster Wheels: Vacuum @ Sea Level:
Unpackaged instrument must withstand two impacts under conditions: Phacoemulsification: 0 - 650 mmHg (0 - 867 hPa) max
- 7.6 cm (3 in) free fall onto all four casters Vitrectomy: 0 - 650 mmHg (0 - 867 hPa) max
- 7.6 cm (3 in) tilt drop onto each caster (raise one caster 7.6 cm (3 in) Irrigation / Aspiration: 0 - 700 mmHg (0 - 933 hPa) max
above the floor, then allow device to fall back to normal position) Power IV Pole:
Console Stability: Height Range: 20 to 110 cm
Meet IEC 60601-1 placed on incline of 10 ° from horizontal IOP Controlled Infusion:
Maximum Weights: Range: 26 - 110 mmHg (35 - 150 cmH2O) (35 - 147 hPa)
Rotating Work Surface: 4.55 kg (10 lb) Accuracy: ± 20 % of setpoint or 15 mmHg (20 hPa)
Instrument Tray Arm: 9.1 kg (20 lb) Aspiration Flow Rate: 0 - 60 cc / min (0 - 60 mL / min)
Degree of Protection by Enclosure: Usable Fluid Volume: ≥ 350 cc (350 mL)
Meets IP10 (console), IPX1 (IR remote control), IPX6 (footswitch) as Voice Confirmation:
specified in IEC 60529 and IEC 60601-2-2, clause 201.11.6.5 (footswitch) Range: 0 to 65 dB
IR Remote Control: Tone Volumes @ 1 meter
Method: Infrared Errors/Faults/Invalid Key: 40 to 65 dB, short tone
Channels: 6 Diathermy: 40 to 65 dB, continuous tone
Batteries: (2x) AA Advisory/Time Expire: 0 to 65 dB, short tones
Footswitch: Phaco/Vacuum: 0 to 65 dB, continuous tones
Dimension: 7.6 cm (3 in) tall x 22.9 cm (9 in) wide x 30.5 cm (12 in) deep Valid Key: Factory set and not adjustable
Weight: No greater than 5.4 kg (12 lb) Volume Accuracy: 6 dB
Environmental: Footswitch construction is water tight in compliance with Proportional and Continuous* Reflux @ Sea Level
IEC 60601-1 and IEC 60601-2-2 Pressure Range: 26 to 140 mmHg (35 - 187 hPa)
Electrical: Footswitch is configured for wireless transfer Pressure Accuracy: ± 10 % of setpoint + 5 mmHg (7 hPa)
Channels: 16 *Total available Reflux volume: 7 cc (7 mL) replenishable via Aspiration
AC Electrical Requirements: INTREPID® AutoSert® IOL Injector:
Input Voltage: 100 - 240 VAC 50 / 60 Hz Max Speed: 4.4 mm / s
Maximum Input Current: 10 A
Protection against Electrical Shock: Class I
Classification of All Applied Parts: Type BF
Data Card: USB data stick: 8 Gb min.

Table 1-5 SPECIFICATIONS - This table is a quick reference point to identify basic system specifications,
system requirements, and performance figures.

Abbrev. Description Abbrev. Description Abbrev. Description

ABS Aspiration Bypass System HP Handpiece UL Underwriters Laboratories
AFR Aspiration Flow Rate I/A Irrigation/Aspiration U/S Ultrasound
Asp Aspiration IOL Intraocular Lens USB Universal Serial Bus
BF Body Floating IOP Intraocular Pressure V Volt
BSS Balanced Salt Solution IR Infra Red Vac Vacuum
cc/min Cubic centimeters per minute Irr Irrigation Vit Vitrectomy
Coag Coagulation IVO Infiniti® Video Overlay IEC International Electrotechnical
CPM Cuts Per Minute kg Kilogram Commission
DFU Directions For Use lb Pound IPN1N2 International Protection Code
ESD Electro Static Discharge LCD Liquid Crystal Diode N1 - solid objects (0 to 6, or X - not
FMS Fluidic Management System mmHg Millimeters of Mercury required to be specified)
FTSW Footswitch PEL Patient Eye Level N2 - ingress of water (0 to 8, or X - not
HF High Frequency PPS Pulses Per Second required to be specified)

Table 1-6 ABBREVIATIONS USED WITH THE CENTURION® VISION SYSTEM

1.24
FOR REFERENCE ONLY 8065751772
 Type BF equipment, providing both the
attributes of basic insulation and "floated" Eject FMS
isolation.

Utility light over instrument tray

Follow Instructions for Use
(white figure on blue background)
Connector for
CENTURION® OZil® handpiece
WARNING: The console might
overbalance when it is pushed and its
wheels are immobilized (blocked) Connector for
(black symbol behind lined out red circle) INFINITI® OZil® handpiece

WARNING: Dangerous Voltage Connector for

(black symbols on yellow background) INTREPID® AutoSert® IOL Injector

GENERAL WARNING Connector for

(black symbols on yellow background) Vitrectomy probe tubing

Connector for
Equipotential ground connection INTREPID® Capsulotomy Device

AC Voltage Connector for

Coagulation handpiece

Power stand-by state

for a part of equipment Connector for
Cabled Footswitch

ON (POWER)

MR Magnetic Resonance Unsafe

OFF (POWER)

Fuse Size, Type, and Rating Non-ionizing electromagnetic radiation

T10.0AH/250V

Use appropriate take-back system Date of Manufacture

(see Environmental Considerations in this manual)
Pb notation, if present, indicates lead
content greater than 0.004%. Manufacturer
Pb

REF Catalog Number OSHA recognized NRTL, TUV SUD

America mark, providing electrical safety
SUD certification to North American
SN Serial Number C US requirements for Medical Devices.

Figure 1-2 ICONS USED WITH CENTURION® VISION SYSTEM - Icons identifying modes, functions,
etc., that are used with the Centurion® Vision System are identified in this chart. The icons shown on
this page are for reference only.

8065751772 1.25
FOR REFERENCE ONLY
 REF
®

®
DANGER: RISK OF EXPLOSION IF USED IN THE SN
PRESENCE OF FLAMMABLE
ANESTHETICS.

DANGER: RISQUE D’EXPLOSION. NE PAS

EMPLOYER EN PRESENCE
D’ANESTHESIQUES INFLAMMABLES.

CAUTION: GROUNDING RELIABILITY CAN ONLY

BE ACHIEVED WHEN EQUIPMENT IS
CONNECTED TO AN EQUIVALENT REV
RECEPTACLE MARKED HOSPITAL
GRADE.
215-2216-001 REV B
CAUTION: RISK OF BURNS AND FIRE - DO NOT
USE NEAR CONDUCTIVE MATERIALS.
RENEW ELECTRODE CABLES UPON
EVIDENCE OF DETERIORATION.
Type BF equipment, providing
both the attributes of basic
Label located on rear panel of Centurion® Vision System
insulation and “floated” isolation.

Follow Instructions for Use

Non-ionizing electromagnetic
radiation.

MR Magnetic Resonance Unsafe

Use appropriate
This device complies with part 15 of the FCC
take-back system
rules. Operation is subject to the following two
conditions: (1) This device may not cause
harmful interference, and (2) this device must
accept any interference received, including
WARNING: Dangerous Voltage interference that may cause undesired
® operation

GENERAL WARNING FCC ID: VMCNGPFSW1

IC: 7345A-NGPFSW1
Manufacturer
ALCON LABORATORIES, INC.
For applicable patents, please see the ABOUT Contains:
6 2 0 1 S O U T H F R E E WAY
screen on the monitor during operation. FCC ID: RI7XE61
FORT WORTH, TX 76134-2099 USA
© 2013 Novartis MADE IN USA IC: 5131A-XE61
Contains:
FCC ID: N6C-SDMAN
IC: 4908B-SDMAN
215-2985-001 REV A

Label printed on rear panel of Centurion® Vision System Label located on rear panel of Centurion® Vision System

WARNING: FOR CONTINUED

PROTECTION AGAINST RISK OF FIRE,
T10.0AH/250V REPLACE ONLY WITH SAME TYPE WARNING
AND RATING OF FUSE.
STORE TRAY PRIOR TO
TRANSPORTATION
215-2687-001 REV A

Label printed on power input module Label located on instrument tray

Figure 1-3A LABELING ON CENTURION® VISION SYSTEM - Labels used on the Centurion® Vision
System are illustrated here. The labels on this page are intended for reference only.

1.26
FOR REFERENCE ONLY 8065751772
 (2) "AA" / LR6
Use appropriate
take-back system
REMOTE CONTROL
Follow
SN Instructions for Use

REF 8065751774
Manufacturer
IPX1 ALCON LABORATORIES, INC.
6 2 0 1 S O U T H F R E E WAY
Date of Mfg
FORT WORTH, TX 76134-2099 USA
© 2013 Novartis 0123 MADE IN USA
215-3061-001 REV A

Label located on back of remote control

This device complies with part 15 of

FOOTSWITCH the FCC Rules. Operation is subject to
the following two conditions: (1) This
device may not cause harmful
For applicable patents, please see the “ABOUT”
GENERAL interference, and (2) this device must
screen on the monitor during operation.
accept any interference received
WARNING including interference that may cause
Follow Instructions undesired operation.
for Use Manufacturer
Non-ionizing electromagnetic
ALCON LABORATORIES, INC.
radiation
6 2 0 1 S O U T H F R E E W AY
IPX6 FORT WORTH, TX 76134-2099 USA Use appropriate
Date of Manufacture MADE IN USA take-back system

215-1016-502 REV FCC ID: VMCNGPFSW1

IC: 7345A - NGPFSW1
REF 8065751762 REV CONTAINS
FCC ID: RI7XE61
IC: 5131A-XE61
SN © 2012 Novartis 215-1994-001 REV. P14

Label located on bottom of footswitch

Figure 1-3B LABELING ON CENTURION® VISION SYSTEM - Labels used on the Centurion® Vision
System are illustrated here. The labels on this page are intended for reference only.

8065751772 1.27
FOR REFERENCE ONLY
 12

10 100%
75%
POWER (W)

8 50%
25%

0
10 100 1000
LOAD (OHMS)
COAGULATION POWER GRAPH

12

10

8
POWER (W)

0
0 20 40 60 80 100 120
% POWER
POWER ACROSS 75 OHM LOAD

60

50
PEAK VOLTAGE (V)

40

30

20

10

0
0 20 40 60 80 100 120
% POWER
VOLTAGE (PEAK) OPEN CIRCUIT

Figure 1-4 COAGULATION POWER OUTPUTS - Set coagulation power at the intended output
control setting in the intended operating mode in reference to figures above.

1.28
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
Table 1-7 SUMMARY OF ALCON DEFAULT SETTINGS

Doctor Settings
No. General Doctor Setting Default
3 Patient Eye Level Offset Default (PEL) -5
4 Irrigation Pressure Drop 60
5 Reflux Pressure Offset 30
6 Vent Time 0
7 Continuous Irrigation Mode Default OFF
8 Continuous Irrigation Auto-Off Threshold 5
11 Verify PEL Enabled
12 Estimated Incision Leakage 0
13 AutoSert® Full Extension Offset 0
14 AutoSert® Remote Control Default Preload Lens
15 Vitrectomy Setup ON

IP Settings
No. Phaco IP Doctor Setting Default
1 Phaco IP Longitudinal Pulse Duration 10
2 Phaco IP Vacuum Threshold 95
3 Phaco IP Longitudinal Power 100

Default Procedures
No. Default Procedure Procedure Description Default Steps
1 Procedure 1 Divide and Conquer PrePhaco, Sculpt, Quad, Epi, Cortex, Polish, Visco
2 Procedure 2 Phaco Chop PrePhaco, Chop, Epi, Cortex, Polish, Visco
3 Procedure 3 Vitrectomy Vitrectomy (Anterior Vitrectomy Mode),
Vitrectomy (Epinucleus Removal Mode),
Vitrectomy (I/A Cut Mode),
Vitrectomy (Peripheral Iridectomy Mode),
Vitrectomy (Visco Aspiration Mode)

Active Irrigation Surgical Parameters

No. Procedure Surgical Parameter Default
1 IOP Ramp Time 1.0

I/A Step Passive Irrigation Surgical Parameters

No. I/A Step Surgical Parameter Default
1 Irrigation Pressure 78

I/A Steps Active Irrigation Surgical Parameters

No. I/A Step Surgical Parameter Default
1 Flow Compensation 1.0

I/A Steps Fluidics Parameters

Cortex Polish Visco
B/E Range 2 IOP 20/55 20/55 20/55
Control in Range 1 IOP Fixed Fixed Fixed
Control in Range 2 IOP Fixed Fixed Fixed
B/E Vacuum 0/500 0/20 0/650
Control in Range 2 Vacuum Linear Linear Fixed
B/E Asp Rate 0/35 0/10 0/50
Control in Range 2 Asp Rate Fixed Linear Linear
Vacuum Rise Time 0 0 0

Phaco Step Passive Irrigation Surgical Parameters

No. Phaco Step Surgical Parameter Default
1 Irrigation Pressure 95

Phaco Step Active Irrigation Surgical Parameters

No. Phaco Step Surgical Parameter Default
1 Flow Compensation 1.0

8065751772 1.29
FOR REFERENCE ONLY
UltraChop Phaco Steps Active Irrigation Surgical Parameters
No. Phaco Step Surgical Parameter Default
1 Flow Compensation 1.0

Phaco Steps Fluidics Parameters

PrePhaco UltraChop Chop Sculpting Quadrant Epinucleus Flip
B/E/E IOP 20/55/55 20/55/55 20/55/55 20/55/55 20/55/55 20/55/55 20/55/55
Control in Range 1 IOP Fixed Fixed Fixed Fixed Fixed Fixed Fixed
Control in Range 2 IOP Fixed Fixed Fixed Fixed Fixed Fixed Fixed
Control in Range 3 IOP Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E/E Vacuum 0/180/180 0/380/380 0/380/380 0/ 80/80 0/380/380 0/380/ 380 0/380/380
Control in Range 2 Vacuum Fixed Fixed Fixed Fixed Fixed Linear Fixed
Control in Range 3 Vacuum Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E/E Asp Rate 0/30/30 0/40/40 0/40/40 0/23/23 0/40/40 0/30/30 0/40/40
Control in Range 2 Asp Rate Fixed Fixed Fixed Fixed Fixed Linear Fixed
Control in Range 3 Asp Rate Fixed Fixed Fixed Fixed Fixed Fixed Fixed
Vacuum Rise Time 0 0 0 0 0 0 0

Phaco Step Surgical Parameters

No. Phaco Step Surgical Parameter Default
1 Phaco IP ON
2 Phaco Mode Continuous

Continuous Phaco Mode Parameters

PrePhaco UltraChop Chop Sculpting Quadrant Epinucleus Flip
B/E Longitudinal 0/0 0/0 0/0 0/0 0/0 0/0 0/0
Control Longitudinal Linear Linear Linear Linear Linear Linear Linear
B/E Torsional 0/20 0/60 0/60 0/60 0/60 0/60 0/60
Control Torsional Linear Linear Linear Linear Linear Linear Linear

Pulsed Phaco Mode Parameters

PrePhaco UltraChop Chop Sculpting Quadrant Epinucleus Flip
B/E Longitudinal 0/0 0/0 0/0 0/0 0/0 0/0 0/0
Control Longitudinal Linear Linear Linear Linear Linear Linear Linear
B/E Torsional 0/20 0/60 0/60 0/60 0/60 0/60 0/60
Control Torsional Linear Linear Linear Linear Linear Linear Linear
B/E Longitudinal DC 0/0 0/0 0/0 0/0 0/0 0/0 0/0
Control Longitudinal DC Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E Torsional DC 0/80 0/80 0/80 0/80 0/80 0/80 0/80
Control Torsional DC Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E Pulse Rate 1/20 1/20 1/20 1/20 1/20 1/20 1/20
Control Pulse Rate Fixed Fixed Fixed Fixed Fixed Fixed Fixed

Burst Phaco Mode Parameters

PrePhaco UltraChop Chop Sculpting Quadrant Epinucleus Flip
B/E Longitudinal 0/0 0/0 0/0 0/0 0/0 0/0 0/0
Control Longitudinal Linear Linear Linear Linear Linear Linear Linear
B/E Torsional 0/20 0/60 0/60 0/60 0/60 0/60 0/60
Control Torsional Linear Linear Linear Linear Linear Linear Linear
B/E Longitudinal On 2/35 2/35 2/35 2/35 2/35 2/35 2/35
Control Longitudinal On Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E Torsional On 2/70 2/70 2/70 2/70 2/70 2/70 2/70
Control Torsional On Fixed Fixed Fixed Fixed Fixed Fixed Fixed
B/E Off 2500/0 2500/0 2500/0 2500/0 2500/0 2500/0 2500/0

IOL Injection Step Parameters

Default
IOL Plunger Type Standard
Initial IOL Injection Rate 1.7
IOL Injection Pause Time 3.0
Beginning IOL Injection End Rate 1.2
Ending IOL Injection End Rate 1.7
Control of IOL Injection Rate Linear

1.30
FOR REFERENCE ONLY 8065751772
Coagulation Step Parameters
No. Coagulation Step Surgical Parameter Default
1 Beginning Coagulation Power 0
2 Ending Coagulation Power 50
3 Control of Coagulation Power Fixed

Vitrectomy Modes Passive Irrigation Parameters

Anterior Vitrectomy Epinucleus Removal Peripheral Iridectomy Visco Aspiration I/A Cut
Irrigation Pressure 65 65 65 65 65

Vitrectomy Steps Active Irrigation Surgical Parameters

No. Vitrectomy Step Surgical Parameter Default
1 Flow Compensation 1.4

Stand-Alone Vitrectomy Step Active Irrigation Surgical Parameters

No. Stand-Alone Vitrectomy Step Surgical Parameter Default
1 Flow Compensation 1.4
2 IOP Ramp Time 1.0

Vitrectomy Modes Active Irrigation Parameters

Anterior Vitrectomy Epinucleus Removal Peripheral Iridectomy Visco Aspiration I/A Cut
B/E/E IOP 20/55 20/55 20/55 20/55 20/55/55
Control in Range 1 IOP Fixed Fixed Fixed Fixed Fixed
Control in Range 2 IOP Fixed Fixed Fixed Fixed Fixed
Control in Range 3 IOP N/A N/A N/A N/A Fixed
Vacuum Rise Time 0 0 0 0 0

Vitrectomy Modes Fluidics Parameters

Anterior Vitrectomy Epinucleus Removal Peripheral Iridectomy Visco Aspiration I/A Cut
B/E/E Vacuum 0/350 0/500 0/350 0/650 0/350/500
Control in Range 2 Vacuum Linear Linear Linear Linear Linear
Control in Range 3 Vacuum N/A N/A N/A N/A Fixed
B/E/E Asp Rate 0/10 0/10 0/10 0/50 0/ 10/20
Control in Range 2 Asp Rate Fixed Linear Fixed Fixed Fixed
Control in Range 3 Asp Rate N/A N/A N/A N/A Fixed

Vitrectomy Modes Parameters

Anterior Vitrectomy Epinucleus Removal Peripheral Iridectomy Visco Aspiration I/A Cut
B/E Range 2 Cut Rate 1/4000 1500/500 N/A/1 1/4000 N/A
Control in Range 2 Cut Rate Fixed Linear N/A Fixed N/A
B/E Range 3 Cut Rate N/A N/A N/A N/A 1/4000
Control in Range 3 Cut Rate N/A N/A N/A N/A Fixed

Irrigation Footswitch Step Passive Irrigation Surgical Parameters

No. Irrigation Footswitch Step Surgical Parameter Default
1 Irrigation Pressure 78

Irrigation Footswitch Step Active Irrigation Surgical Parameters

No. Irrigation Footswitch Step Surgical Parameter Default
1 Beginning Range 2 IOP Target 20
2 Ending Range 2 IOP Target 55
3 Control in Range 1 IOP Target Linear
4 Control in Range 2 IOP Target Fixed

8065751772 1.31
FOR REFERENCE ONLY
 THIS PAGE INTENTIONALLY BLANK

1.32
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION TWO
DESCRIPTION

DESCRIPTION OF CENTURION® VISION SYSTEM

Description
Alcon’s Centurion® Vision System is a multi microprocessor-controlled ophthalmic
surgical instrument with associated memory and input/output (I/O) circuitry. The
system communicates to the user via its Front Panel display, with voice confirmations,
and with tones. An automatic self-test is initiated each time system power is turned
on.

This test checks a variety of functions including the following:

• Host CPU Assembly (including Display&Touchscreen)

• Footswitch Interface
• Multifunction Assembly
• Fluidics Assembly
• Active Fluidics™ Assembly
• Phaco Assembly
• IV Pole Assembly
• Pneumatics Assembly

When the system successfully completes the self-test, it automatically goes into the
Setup mode. If the system fails the self-test, an Event message is displayed.

This section of the manual is broken into two major parts. The first part describes the
console and its accessories. All the parts of the system will be described, including the
display panel, Active Fluidics™ system, gravity fluidics system, connectors, fluidics
interface, footswitch, remote control, and VideOverlay system. The second part of
this section describes the operator interface. This is where the display screens for
system setup, surgery, programming, and dialogs are shown.

Trademark Note
A button, mode, or step labeled OZil®, AutoSert®, or UltraChop refers to a display
screen control used with an OZil® torsional handpiece, INTREPID® AutoSert® IOL
injector, or ALCON® UltraChopper® tip, respectively.

8065751772 2.1
FOR REFERENCE ONLY
 CENTURION® VISION SYSTEM CONSOLE AND ACCESSORIES

DESCRIPTION OF CONSOLE

Fluidics Module

The fluidics module is located in the center of the front panel. The module allows
fast and easy insertion of the Fluidic Management System (FMS; i.e., cassette), and
because the module contains all the connections required, surgery can be started with
minimal delay.

Front Display Panel

and Touch Screen
Rotating Work Surface
and Locking Ring
(Active Fluidics™ Bag Bay
underneath Work Surface)

Standby Power Switch

Convenience Lamp
Handle Bar
Fluidics Module

IR Remote Control
Accessory Drawer
Adjustable Instrument Tray

Speakers (3)

Locking Caster Wheels (4)

Wireless Footswitch

Connectors for
Wired Footswitch

Figure 2-1 The Console - The console contains all the controls, connectors, and communication
devices required by the surgeon to perform cataract lens extraction surgery.

2.2
FOR REFERENCE ONLY 8065751772
 Front Display Panel and Touch Screen
The front display panel tilts and rotates, allowing easy maneuverability during setup and
surgery. For storage and transport, the front panel folds down. The front display is the
user's main source of system control, allowing fingertip command of system functions.

Adjustable Instrument Tray

The Centurion® Vision system provides an adjustable instrument tray within the
sterile field. The tray is capable of accommodating a variety of positions in the
operating room environment—right, left, front, and rear of the surgeon—and the tray
is height adjustable. There are curved metal rods on the tray that allow for creation
of sterile pouches when covered with a sterile tray support cover, and also provide
cradles for the IR remote control. Two rubber clips are built into the tray surface to
neatly secure the handpiece cables and tubing up and off unsterilized surfaces.

CAUTION
The maximum weight allowed on the instrument tray is 9.1 kg (20 lb.)

Front Panel Connectors

The front panel connectors are located on both sides of the fluidics module. The
front panel connectors provide three self-locking phaco handpiece connectors, two
connectors for the INTREPID® AutoSert® IOL Injector, one connector for a bipolar
coagulation handpiece, connectors for the INTREPID® Capsulotomy Device, and
luer lock pneumatic connectors for the Centurion® UltraVit® Probe. The left row
of connectors also includes a utility light for the instrument tray. Symbols near the
connectors facilitate handpiece identification.

The CENTURION® OZil® handpiece is recognized in the top two phaco handpiece
connectors; only the INFINITI® OZil® handpiece is recognized in the bottom. Only one
phaco handpiece can be connected at one time in either connector, unless the UltraChop
feature is enabled in which case the system will accept two phaco handpieces.

Fluidics Module

INTREPID® Capsulotomy Device

Coagulation Handpiece

Utility Light for

Instrument Tray CENTURION® OZil® Handpiece
INTREPID® AutoSert® IOL Injector

Vitrectomy Handpiece
INFINITI® OZil® Handpiece

Figure 2-2 The Front Panel Connectors - The front connector panel allow quick and easy connection
of handpieces and consumables.

8065751772 2.3
FOR REFERENCE ONLY
 Standby Power Switch
This pushbutton switch is used to turn secondary power ON and OFF. If system
freezes and is unresponsive to operator commands, press Standby switch for five
seconds to shut down system, then re-boot.

Accessory Drawer
One drawer allows storage of miscellaneous accessories.

Audio Speakers
Three audio speakers are located on the front and each side of the console. These
speakers produce voice confirmations, in conjunction with multiple tones, to allow the
Centurion® Vision System to communicate with the user. Audible tones are generated
to indicate a change in the operating mode and to alert the operator of certain
conditions such as an occluded line. Additionally, a varied pitch tone is generated to
audibly indicate vacuum levels; the pitch increases as the vacuum level increases.
Speaker volumes are adjustable via the Custom menus.

Power IV Pole and Hanger Active Fluidics™ Bag Bay

for Gravity Fluidics

Rotating Work Surface

Input/Output (I/O) Connector Panel

AC Power Cord Hanger

Irrigating Fluid Escape

Footswitch Hanger

Wireless Footswitch
Charging Station

Primary AC Power Switch

Figure 2-3 Rear and Side Panels

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 Locking Caster Wheels
Four large caster wheels support the Centurion® Vision System. The wheels rotate
360º for ease of system mobility, and all four wheels have a locking lever to secure
the system in place. The wheels should always be locked when the unit is in use, and
unlocked when being moved.

Handle Bar
A handle bar wraps around the sides and back of the Centurion® Vision System, and
should always be used to move it.

CAUTION
The system must be moved carefully, otherwise it could tip over and become
damaged. Do not push or pull the unit by the display, the instrument tray, or the
IV pole. The handle bar is provided for moving the instrument. The unit should be
pulled and not pushed, especially over elevator and door thresholds.

Equipotential Ground Connector

The equipotential ground connector may be used to provide a direct connection
between the Centurion® system and the potential equalization bus-bar of the electrical
installation. This connector complies to the requirements of IEC/EN 60601-1.

AC Power Cord Hanger

Used to store the power supply cord when system is out of use. Located in the middle
of the rear panel.

Primary AC Power Switch

The power module contains an AC power switch, AC power connector, and a fuse
holder. The power module is located at the bottom of the rear panel. A standby power
switch is located at the top of the right side panel.
• AC Power Connector - Power cord from AC power outlet connects here. A
hospital grade power cord must be used.
• Primary AC Power Switch - Connects AC power to power supply.
• Fuse Door - Open the fuse door to gain access to the fuse holder. Refer to label on
back of system to identify fuse size and type.

Footswitch Hanger / Charging Station

When out of use, the wireless footswitch hangs on the back of the Centurion® Vision
System. If used wirelessly, its internal lithium ion battery is charged inductively
through the rear panel. If wired to the system, and system power is turned on, the
footswitch battery is charged through the cable.

Input/Output (I/O) Connector Panel

This panel contains inputs and outputs for Audio input, USB communications,
VideOverlay output (RS232), and Ethernet internet communications (RS422). An
antenna for wireless communications is also located on this panel.

The USB port is provided for Service functions and for backing up and restoring Dr.
memory. Plugging any other USB device into the port is not recommended.

8065751772 2.5
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 Rotating Work Surface
A versatile rotating work surface is provided on the top of the Centurion® Vision
System. When stowed, this work surface covers the Active Fluidics™ bag bay and is
locked in place. When open it allows the user to lower a bag of BSS® irrigating fluid
into the bag bay.

To rotate the work surface and reveal the bag bay, press and hold the locking ring
while pressing sideways on the work surface (see left image in Figure 2-4). The right
image shows the work surface in the open position, allowing access to the bag bay.
Once open, the surface can be rotated until the mechanical lockout feature prevents
further rotation. When Active Fluidics™ technology is used, this lockout feature
prevents inadvertent contact of the work surface against the bag of BSS® irrigating
fluid and its tubing. To return the work surface back to its stowed position, press and
hold the locking ring and press sideways on the work surface.

CAUTIONS
• The maximum weight allowed on the rotating surface is 4.55 kg (10 lb.)
• Work surface must not come in contact with bag of irrigating fluid.

Figure 2-4 Rotating Work Surface - To rotate working surface and gain access to the Active Fluidics™
bag bay, press down on locking ring and rotate work surface out of the way.

2.6
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FLUIDICS ADMINISTRATION

The Centurion® Vision system supports two types of fluidics administration to deliver and
control fluidics fluid pressure: Gravity Fluidics is used for fluid administration using the
power IV pole, and Active Fluidics™ technology is an automated system that administers
fluid from a bag of BSS® irrigating fluid within its bag bay (see Figure 2-3).

Power IV Pole and Hanger for Gravity Fluidics

For gravity fluidics a container of BSS® irrigating fluid is hung from a hanger on top
of the IV pole. Raising and lowering the pole increases and decreases the irrigation
pressure delivered to the tip of the handpiece. The hanger can be installed in 45°
increments by releasing the chrome nut at the bottom of the IV pole, lifting the pole
up, and setting it back down at the desired angle.

Bag Bay for Active Fluidics™ Technology

For Active Fluidics™ technology a bag of BSS® irrigating fluid is compressed
between two plates within the Active Fluidics™ bag bay, located under the rotating
work surface on the top of the console. The pressure created by compressing the
bag of irrigating fluid is monitored to provide an accurate pressure source, allowing
control of intraocular pressure (IOP).

This precise pressure control creates the opportunity to tailor IOP performance
based on surgical preference. There are two functions related to Active Fluidics™
technology which allow the surgeon to tailor IOP performance: Irrigation Factor and
IOP Ramp. These functions are described later in this section of the manual (Fluidics
Controls).

WARNING!
Use of BSS® irrigating fluid bags other than those approved by Alcon for use in the
Active Fluidics™ system can result in patient injury or system damage.

8065751772 2.7
FOR REFERENCE ONLY
DESCRIPTION OF FOOTSWITCH

The Centurion® Vision System utilizes the Centurion® or Laureate® footswitch. The
footswitches have a footpedal and on/off toe switches (horizontal and vertical). The
Centurion® footswitch can be used wirelessly or can be wired to the console, while
the Laureate® footswitch must be wired. When the footswitch is operated wirelessly,
it retains the same functionality as it does when it is wired to the system. The wireless
footswitch is immune to interference from other wireless devices.

The footswitch icon button on the display screen is a graphical representation of the
footswitch connected. When connected, the current footpedal position (0, 1, 2, or
3) is displayed in the center of the icon, and a triangular arrow appears next to the
icon each time a switch is activated. If a footswitch is not connected, a wireframe
footswitch is shown in the status bar and no footpedal position is displayed.

Several functions within the system's operating modes are controlled by the surgeon
using the footswitch. The footpedal enables the surgeon to control irrigation flow,
aspiration rate, capsulotomy activation, phaco handpiece power, vitrectomy cutting,
coagulation power, and IOL injection. The switches are used to turn functions on/off,
to adjust function settings, and to progress through surgical steps.

The footswitch's footpedal and switch adjustments are programmable and are
available by pressing the Footswitch icon button at the top of the display screen, or by
selecting Custom/Doctor Settings/Footswitch (see Figure 2-7).

PRECAUTION: A power reset switch is located in the bottom of the footswitch. In

the case that a reset is required, simply press a cotton swab into the small hole in the
bottom to depress the switch and turn power back on (see Figure 2-9). Re-pairing of
the footswitch will restore the previously-programmed footswitch settings.

CAUTION
Never pick up or move the footswitch by the cable. Dropping or kicking the footswitch
can cause irreparable damage.

Footpedal

Left and Right Toe Switches

Left LED
Connection Status

Right LED
Battery Status

Figure 2-5 The Centurion® Footswitch

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 Footpedal Control
Footpedal positions are shown in Figure 2-6, and footpedal positions/functions in each
mode of operation are listed in Table 2-1. Footpedal control can be programmed for
each doctor's personal preferences by pressing the Footswitch icon button at the top of
the display screen, or by selecting Custom/Doctor Settings/Footswitch (see Figure 2-7).

Depending on the surgery step, the user may have the option to select linear or
fixed footpedal control of a surgical parameter (i.e., aspiration, vacuum, power,
coagulation). With linear footpedal control, the angle of depression within the pedal
range is directly proportional to the parameter output. The parameter output is 0 at
POSITION 0
resting position
POSITION 1
DAL detent 1
TPE
FOO POSITION 2
detent 2
POSITION 3
full footpedal depression

FOOTSWITCH ASSEMBLY

Figure 2-6 Diagram of Footpedal Positions

Footpedal Control of Surgical Functions

Position Position Position Position

Mode 0 1 2 3

Capsulotomy Resting Capsulotomy

Resting Irrigation Irrigation/Aspiration Irrigation/Aspiration/

Phaco Power
Phaco
Continuous Irrigation Irrigation/Aspiration Irrigation/Aspiration
Phaco Power

I/A Resting Irrigation Irrigation/Aspiration

Continuous Irrigation Irrigation/Aspiration

AutoSert® Resting IOL Injection Rate

Injector Initial Velocity, Pause Time, End Velocity

Coag Resting Coagulation Power

Anterior Vit Resting Irrigation Irrigation/Aspiration

Epi Removal Cutting
Peripheral Irid
Visco Asp Continuous Irrigation Irrigation/Aspiration
Cutting

Resting Irrigation Irrigation/Aspiration Irrigation/Aspiration/

Cutting
I/A Cut
Continuous Irrigation Irrigation/Aspiration Irrigation/Aspiration
Cutting

Table 2-1 Table of Footpedal Positions - The footpedal is used by the surgeon to control several
surgical functions. This table shows the functions controlled, dependent on mode of operation
and type of irrigation selected. As the footpedal is depressed it travels from the resting position
into its active positions.

8065751772 2.9
FOR REFERENCE ONLY
 the very start of the treadle range, and the parameter output is equal to the limit value
specified at the end of the treadle range. With fixed footpedal control, the parameter
output is fixed at its limit value throughout the treadle range.

Figure 2-7 Doctor Settings Dialog Screen - Footswitch Tab

Figure 2-8 Doctor Settings Dialog Screen - Button Assignment Selections

Pressing one of the Button Assignment buttons brings up a drop-down menu of functions
that can be activated with the surgeon's toe. Several selections are hidden below the
selections shown here; the slide bar on the right is used to expose the other selections.

2.10
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 Footswitch Range Spans
The footswitch's footpedal spans in each Range are programmable and are available
by pressing the Footswitch icon button at the top of the display screen, or by selecting
Custom/Doctor Settings/Footswitch (see Figure 2-7). The span of Range 0 is always
set at 0 to 5 % of the footpedal range, while Ranges 1, 2, and 3 can be changed in the
Footswitch Range Spans (%) window.

Detent
Footpedal detents identify the transition from one footpedal position to another. When
turned On, the footpedal vibrates when pressing through the detent from one position
into the next. The vibration power can be adjusted up and down with the two Strength
arrow keys.

Toe Switch Control

The footswitch has left and right toe switches that are assigned to control various
surgical functions. The two toe switches operate horizontally and vertically, each
direction actuating a function switch, controlling up to four system functions.

If the footpedal is not depressed, any mutually exclusive switch may be engaged. If
the footpedal is depressed, certain switches may or may not be allowed to engage.

Button Assignment
Footswitch button assignments are programmable and are available by pressing
the Footswitch icon button at the top of the display screen, or by selecting Custom/
Doctor Settings/Footswitch (see Figure 2-7). From this screen, press one of the blue
oval buttons next to the footswitch and select a function from the dropdown list (see
Figure 2-8).

The left horizonal switch is the only switch with a factory default action: Reflux. The
Reflux function can be selected for another switch, allowing the left horizontal switch
to be given another function. The Reflux function must always be assigned to a switch.

The other three switches are listed as None by default, their functions are mutually
exclusive, and each must be programmed by the user. When a switch is given a function
already designated to another switch, the other switch is given a None designation.
Choices are Reflux, Irrigation Pressure+, Irrigation Pressure-, Irrigation Pressure +/-,
Continuous Irrigation, Step+, Step-, and None.

8065751772 2.11
FOR REFERENCE ONLY
 • Reflux
The Reflux switch has triple functionality. In most modes of operation the switch
function is Reflux, while within the AutoSert® injector step the switch function is to
Retract the plunger. One other exception is that in the Capsulotomy step it is used to
Enable the capsulotomy function. At least one toe switch must be dedicated to the
Reflux function.

Reflux: The default reflux pressure is equal to the current bottle height IOP
pressure. The reflux pressure can be increased using the Reflux Offset control in the
Custom/Doctor Settings/Fluidics menu. In all cases, reflux is not available when the
footpedal is depressed, and is not available in a Coagulation step.

Retract: In the AutoSert® injector step this switch moves the plunger in a reverse
direction. Control of this function is not allowed while the footpedal is depressed.

Enable: In the Capsulotomy step this switch enables the capsulotomy function.

• Irrigation Pressure+, Irrigation Pressure-

When using gravity fluidics, a toe switch can be selected to move the IV pole up and
down to increase or decrease the irrigation pressure. These toe switch assignments are
not functional when Active Fluidics™ technology is in use.

• Irrigation Pressure +/- When using gravity fluidics, this switch assignment is used
to increase irrigation pressure by pressing and releasing the switch, and to reduce
irrigation pressure by pressing and holding the switch. This toe switch assignment is
not functional when Active Fluidics™ technology is in use.

• Continuous Irrigation
Delegating Continuous Irrigation to a switch on the footswitch allows the user to turn
Continuous Irrigation on and off, whether or not it is enabled for the selected doctor.

• Step+, Step–
A switch may be assigned as step advance (Step+) or step back (Step–). The Setup,
Coagulation, and Anterior Vitrectomy steps are excluded from this stepping sequence.
If step advance or step back is assigned, when the switch is pressed, the next or
previous step to the current step is selected in the surgery menu.

• None - This selection is made to eliminate functionality from the switch.

Vit Cutter Button Dual Assignment

When in Anterior Vitrectomy mode of operation, a selected footpedal button can be
assigned the function of enabling and disabling the vitrectomy cutter function. This
button, when in other modes, has a different assignment.

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 Footswitch Status LEDs
Two LEDs, one on the left and one on the right of the footpedal heel, illuminate to
indicate footswitch status. The following table shows the LED display patterns with
respect to the footswitch's operation state.

Left LED Indicating Connection Status with Centurion® System

Color and Behavior Description

Solid Blue Connected (wired or wireless)
Off When footswitch is in wireless mode and not engaged*, or in
wireless mode and does not hear beacons from console, or in
shipping state

Right LED Indicating Battery Status

Color and Behavior Description

Solid Green Battery level > 40 % of usable range
Solid Yellow Battery level ≤ 40 % of usable range
Blinking Green Battery level > 40 % while charging
Blinking Yellow Battery level ≤ 40 % while charging
Off When footswitch is in wireless mode and not engaged*, or in
shipping state

* LEDs remain on/blinking for a few seconds after disengagement of the footswitch; i.e., not
pressing on the footpedal or any of the footswitch buttons.

Table 2-2 Footswitch Status LEDs

Charging Footswitch Battery

The footswitch battery can be charged using two different methods:
• The footswitch can be charged wirelessly by cradling it on Centurion® system
footswitch hanger on the rear panel of the console.
• The footswitch can be charged by cabling it to the connector at the bottom of the
Centurion® front panel. With system power turned on, the battery will be charged
through the cable.

Pairing Footswitch with Centurion® System

To change the wireless channel for the footswitch, the footswitch must first be cradled
onto the back of the system. This "pairs" the footswitch with the system and allows
the wireless channel to be changed in the Custom / System Settings / Wireless tab.
Note that since the wireless footswitch and the Surgical Guidance System (SGS)
device share the same network, changing the wireless channel for the footswitch will
require a re-pairing of the SGS device.

8065751772 2.13
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 Footswitch Floor Security
The Centurion® footswitch has four spring-loaded ball plungers at each corner of the
bottom plate (see Figure 2-9). These ball plungers are designed to allow easy sliding
of the footswitch on a smooth floor, and yet still offer secure floor gription when the
weight of the surgeon's foot is resting upon it.

The weight of the surgeon's foot on the footswitch causes the spring-loaded
ball plungers to collapse, allowing the footswitch to rest on its rubber sole, thus
preventing it from sliding on the floor. The tension of the spring-loaded ball plungers
is adjustable to the surgeon's preference using a wide, flat-tip screwdriver. Simply
place the screwdriver directly on top of the ball and press down until the screwdriver
tip settles into the screw slot, then turn clockwise or counterclockwise to increase or
decrease the spring tension.
Spring-Loaded Ball Plungers

Rubber Sole

Reset Switch

Spring-Loaded Ball Plungers

Figure 2-9 Bottom of Centurion® System Footswitch

Cabled Footswitch Connectors

The Centurion® footswitch can be wired to the Centurion® Vision System, while
the Laureate® footswitch must be wired. Each footswitch cable has its own unique
connector at the bottom-center of the Centurion® system's front panel (see Figure 2-10).

Footswitch Connectors

Centurion® System

Laureate® System

Figure 2-10 Cable Connectors for Cabled Footswitches

2.14
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DESCRIPTION OF IR REMOTE CONTROL

The IR remote control for the Centurion® system can be used in one of two ways.
It can be cradled in the curved metal rods that extend from the instrument tray, and
operated under the sterile tray support cover supplied in the disposable pack; this
offers the Scrub Nurse or Sterile Assistant access to the controls from the sterile field.
Alternatively, the Circulating Nurse can operate the remote control outside the sterile
field. Programmability and custom user setup features are functions which are not
accessible from the remote control.

CAUTION
Do not sterilize the remote control as it will damage the unit.

Remote Control Keys and Buttons

The remote control allows the user to quickly navigate procedure steps and make
simple parameter value adjustments (see Figure 2-11). The following describes the
remote control keys and buttons with the function of each, and explanations of when
they are valid. When a remote control key or button is pressed, a valid or invalid key
tone is generated as appropriate.

• Parameter Selection Button (, , , )

The keys on the remote control Parameter Selection button are pressed to select
parameters for adjustment, and to select Coag and Vit steps. The current selection
on the display screen is indicated with a yellow border. With this button the user can
move up, down, left, and right to select the desired parameter. This button is valid
when the footpedal and/or a footswitch button is up or depressed, but is invalid when
a dialog is displayed.

• Snap Keys (A, B, C, D, E, F)

Pressing remote control Snap Keys A through F causes the system to snap focus to
various parameter sections on the surgery screen, reducing the number of keystrokes
to invoke control of the desired section. When a parameter section is selected using
the remote control, the affected setting appears with a yellow border (see Figure
2-12), allowing its values to be adjusted using other remote control keys.

Snap Key Parameter Selected

A Top Status Section
B Phaco Parameter Section
C Task Light/Menu Section
D Fluidics Parameter Section
E Fluidics Qualifiers Section
F Coag/Vit Section

Pressing the Remote Control button icon in the upper Status Panel displays the remote
control's six snap navigation buttons (A, B, C, D, E, and F) as an overlay on the
current screen (white letters in center of black buttons, see Figure 2-41).

8065751772 2.15
FOR REFERENCE ONLY
 Parameter Selection Button

Parameter Value
Adjustment Keys

Enter Key

Snap Keys A-F Prv and Nxt

Navigation Keys

Figure 2-11 IR Remote Control - The remote control fits securely on the instrument tray and allows
rotation in any orientation. The sterile tray support cover is then draped over the remote and tray to
maintain the sterile field.

Figure 2-12 Remote Control Snap Keys- Remote control snap keys A through F appear as small
black buttons when the Remote Control icon button at the top of the screen is pressed. In this case
the Remote Control B key was pressed to activate the Torsional (%) setting, as indicated with a yellow
border. Pressing the remote + and – keys changes the torsional % value.

2.16
FOR REFERENCE ONLY 8065751772
 • Parameter Value Adjustment Keys (+, –)
The remote control Parameter Value Adjustment up/down keys affect settings in
the Surgery Control Window that have adjustment arrows (i.e., power, vacuum,
aspiration) and the linear/fixed toggle buttons. When a surgical parameter is selected
via the Parameter Selection button or remote control, a yellow border indicates that
the item is selected; the Parameter Value Adjustment up/down keys can then be used
to adjust its value.

• Prv and Nxt Navigation Keys (, )

The remote control Previous (Prv) and Next (Nxt) Navigation keys are used to
move left and right through the Setup Step buttons and the Surgery Menu steps. A
Navigation key can also be used in an information dialog to select a button (e.g., OK,
Cancel, Save).

In the Setup Screen, when a Prv key or Nxt key is used to move to a Setup Step
button, the button will be highlighted, but the Enter key must be pressed to activate
the button.

In the Surgery screens, when a step is selected using the Prv key or Nxt key on the
remote control, the step is immediately selected. The Navigation keys move the
remote focus to the left or right, wrapping when the end is reached.

• Enter Key (  )
The remote control Enter key is used to execute a selection after highlighting the
selection with the remote's Prv and Nxt Navigation keys.

Remote Control Batteries

When batteries in the remote control are low, a flashing battery low icon will be
displayed next to the remote control display at the top of the screen.

A battery holder inside the remote holds two (2) AA batteries. To replace batteries,
remove the battery cover from the bottom of the remote. Replace old batteries (see
Figure 2-13) and replace cover. Dispose of batteries following local governing
ordinances and recycling plans.

–
+
+ –

Figure 2-13 Battery orientation in remote control

8065751772 2.17
FOR REFERENCE ONLY
 Select Remote Control Channel
The remote control can be configured to operate on one-of-six channels. This feature
allows six remote controls to independently control six Centurion® Vision Systems
operating in the same room or area. Remote controls are factory preset to channel A.
For proper remote operation, the Centurion® Vision System must be set to the same
channel as the remote control.

To select a remote channel, press the Custom key and select System Settings/General
tab. Select the Change Remote Channel button and follow the on-screen instructions
(see Figure 2-14). No additional steps are needed once the remote channel is set, and
only one remote channel is stored per unit.

PRECAUTION: If necessary to distinguish between remote controls, identify the

remote controls and the units with unique labels.

CAUTION
Do not sterilize the remote control as it will damage the unit.

Figure 2-14 Change Remote Channel Dialog

2.18
FOR REFERENCE ONLY 8065751772
HANDPIECES, TIPS, AND INFUSION SLEEVES

Different handpieces, tips, and infusion sleeves are required for different procedural
steps and/or functions. A full selection of handpieces, along with tip styles and sizes
are available. Please contact your Alcon representative for information regarding the
appropriate handpieces, tips, and infusion sleeves for your specific technique and needs.

Following is a general description of the various handpieces, tips, and infusion

sleeves used to perform lens removal procedures.

Phaco Handpieces
Alcon's phaco handpieces integrate irrigation, aspiration and emulsification (see
Figures 2-15 & 2-16). The three functions of the lens extraction step enable the
surgeon to simultaneously maintain or inflate the anterior chamber, emulsify the lens,
and aspirate the lens material from the eye.

These handpieces require no disassembly other than removal of the disposable tubing,
the ultrasonic tip, and the infusion sleeve.

N
TURIO
CEN

Figure 2-15 CENTURION® OZil® Handpiece

Figure 2-16 INFINITI® OZil® Handpiece

8065751772 2.19
FOR REFERENCE ONLY
 Phaco handpieces are used for ultrasonic applications on the Centurion® Vision
System with TurboSonics® tips, including flared, ABS®, and/or ALCON®
UltraChopper® tips. For best OZil® torsional handpiece performance, use tips
recommended by your Alcon representative.

CAUTIONS

Do not test or operate a phaco handpiece unless the tip is immersed in BSS® sterile
irrigating fluid or distilled water or is in surgical use. Irreparable damage to the
handpiece and tip can result if run dry.

Ensure that test chamber is filled with BSS® sterile irrigating fluid before tuning
the phaco handpiece. Tuning a handpiece dry may result in premature tip failure
and breakage.

WARNINGS!

Use of an ultrasonic handpiece other than an OZil ® handpiece, or use of a handpiece

repaired without Alcon authorization, is not permitted, and may result in patient
injury, including potential shock hazard to patient and/or operator.

Use of a phaco handpiece in the absence of irrigation flow and/or in the presence of
reduced or lost aspiration flow can cause excessive heating and potential thermal
injury to adjacent eye tissues.

2.20
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 TurboSonics® Family of Tips
U/S tips are made of medical grade titanium alloy, and are attached to a phaco
handpiece to deliver mechanical energy to the lens, assisting in its removal by
aspiration (with the exception of the ALCON® UltraChopper® tip – see below).
Depending on the needs and technique preferred by the surgeon, various styles of tips
and tip bevels are available (see Figure 2-17). Various U/S tip styles are color coded.

• 0.7 mm and 0.9 mm U/S Tips - The 0.7 mm and 0.9 mm ultrasonic tips are
designed to allow entry through a smaller incision. The 0.7 mm U/S tips are
designed for use only with 0.7 mm infusion sleeves; the 0.9 mm U/S tips are
designed for use only with 0.9 mm infusion sleeves.

• Aspiration Bypass System - The ABS® tip contains a small hole in the distal
portion of the tip’s wall. This helps to maintain fluid flow through the system even
during occlusion of the tip’s main port.

• ALCON® UltraChopper® Tip - This 0.9 mm U/S tip is designed for pre-chopping
only. It is not designed to aspirate lens material.

WARNINGS!
Use 0.7 mm tips with 0.7 mm infusion sleeves; use 0.9 mm tips with 0.9 mm
infusion sleeves. Mismatch of consumable components and use of settings not
specially adjusted for a particular combination of consumable components may
create a patient hazard.

Standard U/S Tip - The TurboSonics® tip with the Kelman® Tip - The Kelman® tip has a bent shaft
round shaft is the original, classical U/S tip shape. which generates torsional ultrasound motion, in addition
to the conventional longitudinal motion, to enhance cutting
efficiency. In addition, the 20 degree bend allows better
visibility during the surgical procedure.
OZil® 12 Tip - Similar to the Kelman® tip, except its bend
is 12 degrees instead of 20. This smaller bend maintains
good torsional cutting efficiency with similar ergonomics
to a straight tip.

Aspiration Bypass System ALCON® UltraChopper® Tip - This tip is similar to a

standard phaco tip, but with a flattened, downward-curved
end to facilitate prechopping. This tip is used for fragmentation
of nuclei for a variety of densities to be used with an ultrasonic
ABS® Intrepid® Balanced Tip – The balanced tip handpiece to separate a cataractous lens into smaller pieces.
has a double bend profile to enhance torsional cutting
efficiency with minimum incision misting and similar
ergonomics to a straight tip. The ABS® tip feature helps
maintain fluid flow, even during occlusion of the tip’s
main port.
Flared ABS® Tip - The Flared ABS® MicroTip and the
Mini-Flared ABS® Tip have a larger proximal port, providing
increased holding force. (Mini-Flared tips have a slightly smaller
proximal port than Flared versions.) Flared tips narrow in the
Tapered ABS® MicroTip - The tapered tip is a combination
middle of the shaft, thus allowing smaller incisions and improving
of the 0.9 mm tip and the flared tip. The shaft inner and
occlusion breaks by reducing outflow from the anterior chamber
outer diameters is equivalent to straight tips, while the
following occlusion breaks. To further enhance performance,
distal end is comparable to flared tips. The tapered
Flared tips also have the Aspiration Bypass System feature.
tip has the improved holding force of a flared tip, and
the same aspiration flow characteristics as a straight tip.

Figure 2-17 TurboSonics® Tips - Shown here are samples of handpiece tips used with Alcon phaco
handpieces.

8065751772 2.21
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 Infusion Sleeves
Infusion sleeves cover the tip of the handpiece to provide irrigating fluid to the
anterior chamber of the eye during surgery (see Figure 2-18). Infusion sleeves are
used with phaco handpieces, and with the Ultraflow™* II I/A handpiece. Infusion
sleeves must be correctly matched to the specific tip type (see the following
descriptions).

Depending on the needs and technique preferred by the surgeon, various styles of
infusion sleeves are available.
INFUSION SLEEVE

CENTURION

Figure 2-18 CENTURION® OZil® Handpiece with Infusion Sleeve.

• Standard MicroSmooth® Infusion Sleeves - These are the original infusion sleeves.
Standard infusion sleeves are 0.9 mm (purple), to be used with 0.9 mm tips.

• INTREPID® Ultra Infusion Sleeves - Ultra infusion sleeves have a smaller shaft
diameter than original infusion sleeves. The smaller shaft diameter of the Ultra
infusion sleeves is compatible with a 2.2 mm incision. Ultra infusion sleeves are
available in 0.9 mm (rose) and 0.7 mm (yellow). Refer to consumable pack DFU
for compatible tips.

• INTREPID® Nano Infusion Sleeves - Nano infusion sleeves have a smaller shaft
taper and proximal outer diameter than Ultra infusion sleeves. The smaller proximal
OD and decreased taper of the Nano sleeves are compatible with a smaller 1.8 mm
incision. Nano infusion sleeves are available in 0.9 mm (orange) and 0.7 mm
(gray). Refer to consumable pack DFU for compatible tips.

WARNINGS!

Use 0.7 mm tips exclusively with 0.7 mm infusion sleeves; use 0.9 mm U/S tips
exclusively with 0.9 mm infusion sleeves. Mismatching U/S tips and infusion
sleeves may create potentially hazardous fluidic imbalances.

Mismatch of consumable components and use of settings not specially adjusted for
a particular combination of consumable components may create a patient hazard.

Read all packaging and Directions for Use supplied with the consumable packs
prior to their use.

2.22
FOR REFERENCE ONLY 8065751772
 Ultraflow™* II I/A Handpiece
The Ultraflow™* II handpiece is used in I/A mode to maintain chamber pressure with
irrigation while removing cortical material via aspiration (see Figure 2-19). Refer to
the Ultraflow™* II I/A Handpiece DFU for more information.

WARNINGS!

Use of non-ALCON® surgical reusable or disposable I/A handpieces that do not

meet Alcon surgical specifications, or use of an Alcon handpiece not specified for
use with the Centurion® Vision System, may result in a fluidic imbalance. This, in
turn, may cause a shallowing or collapsing of the anterior chamber.

Exceeding the recommended level of 100 mmHg (133 hPa) with a 0.5 mm or larger
I/A tip may cause anterior chamber shallowing and/or incarceration or tearing of
the posterior capsule.

Perform visual inspection of accessories for burrs or bent tips prior to use.

I/A tips are not to be used with phaco handpieces.

TM

Figure 2-19 ULTRAFLOW™* II HANDPIECE - Shown here is the Ultraflow® II hand-

piece with I/A tip.

8065751772 2.23
FOR REFERENCE ONLY
 INTREPID® AutoSert® IOL Injector

The INTREPID® AutoSert® IOL Injector is intended to deliver qualified AcrySof®

intraocular lenses into the eye following cataract removal (see Figure 2-20). The IOL
injector, after proper preparation with a loaded, single use cartridge, gives the surgeon
footpedal control of AcrySof® lens insertion. The IOL injector supports the D/C
cartridge or INTREPID® cartridge and associated lenses. Please refer to the INTREPID®
AutoSert® IOL Injector DFU for qualified cartridge/IOL combinations.

The AutoSert® Injector step does not appear at the bottom of the surgery screen until it
is added through the Custom/Procedure Builder dialog.

When connected, the Centurion® system begins calibrating the IOL injector, and if
successful, it becomes ready for use, changing its icon in the adjustment bar from
gray to green.

The IOL injector comes with a detachable and reusable plunger. Please refer to the
INTREPID® AutoSert® IOL Injector DFU for instructions on proper preparation and
use of the handpiece and plunger.

Figure 2-20 INTREPID® AutoSert® IOL INJECTOR - The AutoSert® Injector gives the
surgeon footpedal control of IOL insertion (single use cartridge with lens
not shown).

CAUTIONS
• Do not ultrasonically clean the AutoSert® IOL Injector connector. Ultrasonic
cleaning of connector will cause irreparable damage.
• Use care when handling AutoSert® IOL Injector, particularly when cleaning. Always
clean AutoSert® IOL Injector over a surface cushioned with a pad or rubber mat.
• Be sure AutoSert® IOL Injector cable connector is dry before connecting it to console.
• Do not immerse AutoSert® IOL Injector in any fluid when plunger is not retracted.
• Do not disconnect cable connector from Centurion® system console until the
AutoSert® IOL Injector plunger is fully retracted.
• As part of a properly maintained surgical environment, it is recommended that
a backup IOL injector be made available in the event the AutoSert® IOL injector
handpiece does not perform as expected.

AutoSert® IOL Injector warnings are listed on next page

2.24
FOR REFERENCE ONLY 8065751772
 WARNINGS!
• The INTREPID® AutoSert® IOL Injector is non-sterile and must be cleaned and
sterilized prior to, and immediately after, each use.
• Never immerse the IOL injector in liquid after autoclaving; allow it to air cool for at
least 15 minutes. Quenching could result in a potentially hazardous condition for
the patient.
• The AutoSert® IOL Injector delivery system is for the implantation of Alcon qualified
AcrySof® foldable IOLs. Unqualified lenses shall not be used with the system. See
INTREPID® AutoSert® IOL Injector DFU or AcrySof® IOL DFU, or contact your Alcon
representative, for qualified lens/cartridge combinations.
• The cartridge/IOL combination listed in the DFU, along with Alcon settings, has
been validated per section 5 of BS EN ISO 11979-3:2006. Appropriate use of injector
handpiece settings is important for successful IOL implantation. Inappropriate use
of settings may lead to a potentially hazardous condition for the patient.
• Fully retract plunger before detaching nosecone from AutoSert® IOL Injector;
otherwise, this could expose non-sterile portion of shaft and result in a potentially
hazardous condition for the patient.
• For the intended IOL to be implanted, the proper Cartridge profile must be selected
from the driving console, and the proper plunger must be attached to the AutoSert®
IOL Injector. Failure to do so can result in a potentially hazardous condition for patient.
• The metal reusable plunger must be sterilized after each use. The reusable plunger
is to be installed onto the handpiece or into the wrench prior to sterilization.

FOR REFERENCE ONLY

8065751772 2.25
 Centurion® UltraVit® Probe

The Centurion® system supports the 23 gauge Centurion® UltraVit® vitrectomy probe
(see Figure 2-21). The probe is a sterile, single-use, vitreous cutter which provides
for aspiration and cutting. An irrigating cannula is provided in each pack to allow for
bimanual irrigation.

The 23 gauge Centurion® UltraVit® probe supports higher cut rates by utilizing an
additional pneumatic actuation line.

Each probe is completely preassembled and requires no lubrication or cleaning prior

to surgery. These guillotine vitreous cutters are intended for single use only.

Irrigating Cannula Male Luer

Irrigation Tubing
From Centurion®
Fluidic Management
Centurion® UltraVit® Probe System (FMS)
Male Luer Female Luer
Aspiration Tubing

Gray Fitting
Clear
Pneumatic Tubing Connect to Centurion®
Front Connector Panel
Black Fitting
Black Striped

Figure 2-21 VITRECTOMY PROBES - The 23 gauge Centurion® UltraVit® probe operates
at up to 4000 cpm and utilizes two pneumatic lines. The probe is packaged with an
irrigating cannula.

VITRECTOMY PROBE WARNINGS!

Do not test or operate vitrectomy probes unless tip of probe is immersed in
BSS ® sterile irrigating solution or distilled water or is in surgical use. Irreparable
damage to the probe and tip can result if run dry.

Connect pneumatic tubing connectors from vitrectomy probe to console prior to

initiating prime of probe. Initiating prime of the vitrectomy probe, or running the
vitrectomy system, with one or both pneumatic connectors disconnected may cause
the flow of non-sterile air over the sterile field for a brief moment.

After filling and testing, and before surgical use, verify that the probe is properly
actuating and aspirating. This may require lowering cut rate to achieve good
visualization. The port should always remain in open position in footpedal position 1.
If cutting port is partially closed while in position 1, replace the probe. Prior to entry
into the eye, and with tip of probe in sterile irrigating solution, the surgeon
should step on the footpedal for visual verification that the probe is cutting:
• If the cutter is observed to not fully close, or does not move when the probe
is actuated, replace the probe.
• If cutting port is partially closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the probe tip during
priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during the surgical
procedure, stop immediately and replace the probe.

2.26
FOR REFERENCE ONLY 8065751772
 INTREPID® Capsulotomy Device (future feature)

The Centurion® system supports the INTREPID® Capsulotomy Device (ICD) used
to perform capsulorhexis in the Capsulotomy mode of operation (see Figure 2-22).
The ICD uses cauterization by means of a resistive heating element to create the
capsulotomy and is indicated for use in the creation of an anterior capsulotomy during
anterior segment ophthalmic surgery and implantation of a 6.0 mm IOL.

Please refer to INTREPID® Capsulotomy Device DFU for warnings and details on operation.

The ICD is a single-use device provided sterile to the end user, and is packaged to
allow aseptic transfer into the sterile field by a non-sterile person according to its DFU.

Figure 2-22 INTREPID® Capsulotomy Device - The ICD is a single-use instrument used
to perform a capsulotomy through the means of a resistive heating element at the tip
of the handpiece. The heating element retracts into the handpiece tip during insertion
into the eye, then is extended from the tip for capsulorhexis.

Bipolar Coagulation Accessories

Bipolar coagulation handpieces and cables are not sold by Alcon. See accessories list
in Section Six of this manual for bipolar cables approved for use with the Centurion®
Vision System.

8065751772 2.27
FOR REFERENCE ONLY
FLUIDIC MANAGEMENT SYSTEM

Description
The Fluidic Management System (FMS; i.e., cassette) is an interface between the
Centurion® console (Fluidics Module) and the surgical handpiece (see Figure 2-23).
It is used to regulate BSS® irrigating fluid to the handpiece, aspirate debris from the
handpiece, monitor irrigation and aspiration pressure, and deposit the debris in a
sealed drainage bag for disposal. This single assembly contains a rigid plastic fluidic
chamber, non-invasive pressure/vacuum sensor, drain bag, BSS® irrigating fluid
administration line, and irrigation and aspiration handpiece tubing.

Two types of FMS can be used with the Centurion® Vision System. For Active Fluidics™
technology the FMS has short, clear tubing with an irrigation spike that plugs into a bag
of BSS® irrigating fluid. For Gravity Fluidics the FMS has long, clear tubing with a drip
chamber that plugs into a container of BSS® irrigating fluid hanging from the IV pole.

The type of FMS inserted is automatically identified by the system when it is

inserted into the fluidics module. Inserting the FMS into the console fluidics module
establishes fluidics system connections, contributing to quick and easy surgical setup.

Finger grip for inserting and removing FMS

Rigid plastic fluidic chamber

Locking connector (white) on

irrigation tubing connector (black)

Blue connector on
aspiration tubing

Spike on end of
BSS® irrigating fluid
administration line is
for Active Fluidics™ technology.

Gravity fluidics uses

a spike/drip chamber on
end of BSS® irrigating fluid
administration line.

Drain Bag

Figure 2-23 Fluidic Management System - The FMS is inserted into the Fluidics Module on
the front of the console to establish fluidics system connections. Shown here is the FMS
for Active Fluidics™ technology; the FMS for gravity fluidics contains longer irrigation
tubing and a spiked drip chamber at the end of the irrigating fluid administration line.

2.28
FOR REFERENCE ONLY 8065751772
CONSUMABLE PACK CONFIGURATIONS

The family of Centurion® packs consist of various combinations of fluidic

management systems (FMS), handpiece tips, infusion sleeves, and other components.
Consumable items used with the Centurion® Vision System during surgery are
designed to be used once and then discarded, unless labeled otherwise.

Please contact your Alcon Sales representative for complete up-to-date listings, and
for in-service information prior to initial use of Alcon packs. All Centurion® packs
contain Directions for Use (DFU). It is important to read and understand the DFU's
prior to use.

In all cases, the instrument setup instructions contained in the manual should be
thoroughly understood prior to using any of the pack configurations.

PRECAUTION: If an inconsistency exists between the instructions in the operator's

manual and the Directions For Use (DFU) supplied with a consumable pack or
accessory, follow the DFU.

Custom Pak™* Surgical Procedure Pack Configurations

To better serve our customers we offer the opportunity for surgeons to specify a
Custom Pak™* surgical procedure pack for their own individual needs. Please contact
your Alcon Sales representative for more information on how to design your own
Custom Pak™* surgical procedure pack.

WARNINGS!

Mismatch of consumable components and use of settings not specially adjusted for a
particular combination of consumable components may create a patient hazard.

Do not use packs that have exceeded the expiration date.

Sterile disposable medical devices should not be reused! These components have
been designed for one time use only; do not reuse.

The equipment used in conjunction with the Alcon disposables constitutes a

complete surgical system. Use of disposables other than Alcon disposables may
affect system performance and create potential hazards, and if it is determined to
have contributed to the malfunction of the equipment under contract, could result
in the voidance of the contract and/or invoicing at prevailing hourly rates.

8065751772 2.29
FOR REFERENCE ONLY
 Centurion® Fluidic Management System Packs
When performing a phacoemulsification procedure, one-of-two Centurion® FMS packs
with handpiece tip is used. One FMS pack is specific for Active Fluidics™ technology,
(when using bag of BSS® irrigating fluid in the bag bay) and the other is for gravity
fluidics (when using container of BSS® irrigating fluid hanging from IV pole). The pack
can contain all the items listed below:

• Fluidic Management System (FMS) - This single assembly consists of a

BSS® irrigating fluid administration line (tubing with a spike for Active
Fluidics™ technology, or spike/drip chamber for gravity fluidics), irrigation
tubing and aspiration tubing, a plastic body (containing pump, valves, and
sensors), and a drainage bag (maximum capacity of 500 cc [500 mL]).
Inserting the FMS into its console receptacle establishes the Centurion®
fluidic system, allowing quick and easy surgical setup.

• U/S Tip with Tip Holder/Wrench - The tip attaches to the ultrasonic
handpiece. Securely tighten the tip with the all-in-one tip/wrench assembly,
then remove the wrench from the tip. Several tip designs are available.

• Infusion Sleeve - This single-piece silicone sleeve fits over the handpiece
tip to provide irrigating fluid into the eye, protection to the surrounding
tissues, and fluidic balance. Two infusion sleeves are provided; one to be
used with the phaco handpiece/tip, and a second to be used with the I/A
handpiece/tip.

• Test Chamber - The test chamber is a small elastomeric cap that fits over
the handpiece tip to facilitate a functional irrigation and aspiration check
of the handpiece and instrument prior to surgery.

• I/A Tip Wrench - A separate wrench is required to securely fasten the I/A tip
to its handpiece, and also to remove the tip when the surgery is completed.

• Tray Support Cover - The tray support cover is a sterile plastic bag that is
placed around the instrument tray and support arm. The cover is used to
form a pouch in the tray to provide storage for the handpiece and tubing
during surgery.

• Directions for Use (DFU) - Instructions for setup and removal of pack
contents (not shown).

2.30
FOR REFERENCE ONLY 8065751772
VIDEOVERLAY SYSTEM (optional item)

Overview
The VideOverlay system accepts operating parameters from the Centurion® Vision System
and overlays that information onto video accepted from the microscope camera (see Figure
2-24). The VideOverlay system then outputs a video signal to a monitor and/or VCR for
retrospective viewing.

For a complete description of the High Definition VideOverlay system, please refer to the
operator's manual addendum which accompanied the High Definition VideOverlay system.

The VideOverlay system is powered by an external power supply. The external power supply
can operate from a 100 VAC to 240 VAC source, and provides an output of 12 VDC at 1.25
amps to power the VideOverlay system.

WARNINGS!
• Do not remove VideOverlay cover; there are no user-serviceable parts inside. Refer
servicing to qualified service personnel.
• Patient environment defines a volume in which intentional or unintentional contact can
occur between the patient and parts of the equipment or between the patient and other
persons touching parts of the equipment. Please ensure that the VideOverlay system is
outside the patient environment.

CAUTIONS
• Do not use multiple portable socket outlets with this system.
• Use only Alcon-supplied serial cable to connect Centurion® Vision System to VideOverlay
system.

PRECAUTIONS:
• This unit is not a medical device and should be located/stored with other video equipment
(i.e., VCR, monitor, etc.).
• When connected to the Centurion® Vision System, the VideOverlay system does not increase
the leakage current of the Centurion® Vision System.
• The VideOverlay system is for information purposes only, and is not intended to substitute for
the Centurion® Vision System display.

To set up the HD IVO, refer to documentation that came with HD kit.

POWER MMC COMM PAL NTSC

MMC Sensor
On = MMC Card Detected NTSC Video Source
Off = MMC Card Not Detected

Send & Receive PAL Video Source

Flashing = Actively Communicating

Figure 2-24 Standard VideOverlay Front Panel

8065751772 2.31
FOR REFERENCE ONLY
 Setup For Standard VideOverlay System

1. Ensure electric power to all systems is turned OFF. Attach the 12 V end of the external
power supply to the VideOverlay system.

2. Attach the appropriate wall outlet adapter (USA, United Kingdom, Australia, or Europe)
to the AC end of the external power supply, and plug it into an appropriate wall outlet
(see Figure 2-26).

3. The VideOverlay system can operate using either Composite Video inputs/outputs or
S-Video inputs/outputs. Appropriate cables should be used to configure the VideOverlay
system. Connect the microscope camera output to the Composite or S-Video input of the
VideOverlay system (see Figures 2-25 & 2-27).

PRECAUTION: If the microscope camera output has an RCA or BNC connector, connect
the camera output to the VideOverlay Composite input. Do not use an adapter cable to
connect the camera output to the VideOverlay S-Video input or loss of color will occur.

4. Connect the Composite or S-Video output of the VideOverlay system to a monitor or a

VCR. The video output selected must be the same configuration as that used for the video
input (Composite or S-Video).

5. With the video output connected to a monitor, turn the monitor and microscope camera
power ON, and leave the VideOverlay system power OFF. If the video input and output
cables are connected properly, the microscope camera image will appear on the monitor.

6.
Connect the serial cable between the VideOverlay system and Centurion® Vision System.

7. Turn Centurion® Vision System power ON. Turn VideOverlay system power ON with its
rear panel switch. The MMC light and either the PAL or NTSC Video source light should
be illuminated (if not illuminated, check power supply connections).

8. With the Centurion® system touchscreen interface running, make sure the Send &
Receive light blinks (if not blinking, check serial cable).

9. Observe the monitor video display. If the system does not operate correctly, contact an
Alcon Technical Service representative.

COMPOSITE S-VIDEO
VIDEO
INFINITI™ POWER

ON
12VDC
IN OUT IN OUT 1.25A
OFF

Figure 2-25 VideOverlay Rear Panel

2.32
FOR REFERENCE ONLY 8065751772
 USA, Japan, China United Kingdom Australia Europe

External Power Supply

Figure 2-26 Wall Outlet Adapters

Camera

Eye

Centurion® Vision System Rear Panel

Camera output to VideOverlay system
input (S-Video or Composite Video)

NOTE: On the VideOverlay system you Serial cable from

must use either Composite in/out or Centurion® Vision System
S-Video in/out. Do not use use to VideOverlay System
C-in/S-out, or S-in/C-out.
To Wall Outlet
COMPOSITE S-VIDEO
VIDEO
INFINITI™
POWER

ON
12VDC

External
1.25A
IN OUT IN OUT OFF
Power Supply
VideOverlay Rear Panel

VideOverlay system output (Composite Video or S-Video)

to VCR or Monitor input

VCR output
VCR to Monitor input ®

Monitor

Figure 2-27 Standard VideOverlay Connection Diagram

8065751772 2.33
FOR REFERENCE ONLY
 HD Camera
with Component Video

Eye
Centurion® Vision System Rear Panel

To Wall Outlet

Monitor

Serial cable from

External
Centurion® Vision System
Power Supply
to HD VideOverlay
Sony PDW-70MD

HD & SD COMPONENT S-VIDEO CVBS

ANTENNA
HD-SDI OUT
SD-SDI
6.0VDC
2.1A ON
IN

USB RS232 PWR OFF

Y Cb CR CONFIG
IN OUT

HD VideOverlay

Figure 2-28 High Definition VideOverlay Connection Diagram

2.34
FOR REFERENCE ONLY 8065751772
 CENTURION® VISION SYSTEM OPERATOR INTERFACE

FRONT DISPLAY PANEL AND TOUCH SCREEN

The Centurion® Vision System front display panel and touch screen has a flat, non-
glare surface, and is mounted above the console. For ease of viewing the display
panel swivels and rotates, and it folds down into a protected position for storage.

Control buttons are located within the active touch screen area. There are three basic types
of pushbuttons on the display screen: up/down arrow buttons, momentary buttons, and
slider buttons. The user can press and hold the up/down arrow buttons until the desired
adjustment is complete, he can press the momentary buttons with a single push-and-
release to activate a function, and he can press and hold slider buttons while moving the
slider until the desired adjustment is complete.

The Centurion® Vision System emits an audible tone to indicate button activation.
Activation of a valid touchscreen button or remote control button results in a valid key
tone; an invalid button results in an invalid key tone, and sometimes its icon symbol is
ghosted to indicate an invalid function.

There are three types of display screens: the Setup screen, Surgery screens, and Dialogs.
• The Setup screen is used to prepare for surgery; i.e., priming the fluidic
management system and testing the handpiece.
• Surgery screens contain special surgical settings for each of the current surgical
procedures. Pressing the touch screen buttons (or footswitch or remote control)
allows the user to adjust the settings for his current step.
• Dialogs are displayed as a result of selecting an option from the Custom drop
list (i.e., Doctor Settings, System Settings, Procedure Builder, etc.) or pressing
the CDE or Remote buttons. Dialogs enable the user to view and modify system
settings, doctor settings, and some surgical settings. There is another class of
dialogs that are displayed when the user needs to be advised or warned of a
situation, or to indicate progress on a function in the Setup screen.

Initialization Screen

Setup Screen Custom

Surgery Screens

Phaco Irrigation/Aspiration Coagulation Anterior Vitrectomy AutoSert* AutoCap* Fill* Irrigation FS*
• Continuous • Irr/Asp • Coag Vit
• Pulse • Coag 1* Ant Vit*
• Burst • Coag 2* Epi Vit*
• Chop* PI Vit*
• UltraChop* Visco Vit*

* These individual steps can be inserted into the bottom row of steps in a surgery screen using the Custom / Procedure Builder menu.

Figure 2-29 Navigating the Centurion® Vision System User Screens

8065751772 2.35
FOR REFERENCE ONLY
SETUP SCREEN AND ITS FUNCTIONS

The Setup screen is displayed when one of the following occurs:

• The system is powered up and initialization is successful.
• The screen is explicitly invoked by pressing the Setup button from a Surgery screen.
• A Custom dialog screen is exited.
• The FMS is removed while in a surgery screen other than Coagulation.
• A handpiece is selected in a surgery screen and the handpiece is not tuned.
• A valid FMS is inserted while the user is in a surgery screen.

The Setup screen is divided into three sections. At the top is the Status Panel, below
that is the Setup Status Window, and below that are the Setup Steps.

1. Status Panel
The Status Panel (labeled 1 in Figure 2-30) consists of buttons and readouts that are
used to set up the system and then perform surgery. The Status Panel contains the
same data in both the Setup screen and the Surgery screens, discussed later.

1.4 Front Panel

1.2 Procedure Type 1.6 Cumulative Dissipated Energy

1.3 Remote Control 1.5 Footswitch

1.1 Doctor Name

1. Status Panel 1.7 SGS Pairing Indicator

2. Setup Status Window

3. Setup Steps

Figure 2-30 Functional Areas of the Setup Screen Using Active Fluidics™ technology

2.36
FOR REFERENCE ONLY 8065751772
1.1 Doctor Name Button
The Doctor Name button in the Status Panel displays the currently-selected doctor.
When pressed, and also when system is first turned on, this button displays a drop list
of all the doctors entered in the system (see Figure 2-31). The first doctor at the top of
the list is the Alcon Settings doctor, which contains all the Alcon defaults. A summary
of Alcon Settings defaults can be found in Table 1-7.

PRECAUTION: When the selected Doctor Name is Alcon Settings, changes to

settings are temporary; although, when exiting Alcon Settings a dialog appears
allowing the user to save the settings under a new doctor name.

At the bottom of the list is the Manage Doctors selection which allows the user to
add a new doctor to the list, copy a doctor's settings to a new doctor name, rename a
doctor, and delete a doctor from the list. The doctors are listed with the most-recently-
selected doctor in the top position, immediately below Alcon Settings.

An asterisk is placed next to the doctor name if there are unsaved changes to surgical
parameters. For Alcon Settings only, an asterisk appears if there are changes to doctor
settings, but not if the only change is the addition or removal of steps.

WARNING!
Ensure that appropriate Centurion® system parameters and system settings are
selected prior to starting the procedure. Parameter and system settings include, but
are not limited to, mode, power, vacuum, aspiration flow rate, etc.

Figure 2-31 Drop List of Doctors in System

8065751772 2.37
FOR REFERENCE ONLY
 Manage Doctors…
When Manage Doctors is selected from the Doctor Name drop list in the Status Panel
(see Figure 2-31), a dialog window appears with a window for the addition of new
doctors (see Figure 2-32). Pressing the New Doctor button in the dialog prompts an
alphanumeric keypad to appear upon which a new doctor name can be typed and
accepted by pressing the Confirm () button (see Figure 2-33).

A doctor name with preprogrammed settings can be selected and modified from the
Manage Doctors dialog by pressing one of the following buttons (see Figure 2-34):
• Copy Doctor - An alphanumeric keypad appears where the settings used by the
selected doctor can be copied to a new doctor name.
• Rename Doctor - An alphanumeric keypad appears where the selected doctor
name can be changed.
• Delete Doctor - A dialog appears allowing the user to delete the selected doctor
name and its settings.

Figure 2-32 Manage Doctors Dialog

Figure 2-33 Enter Doctor Name Keypad Dialog

2.38
FOR REFERENCE ONLY 8065751772
 Figure 2-34 Manage Doctors Dialog

Figure 2-35 New Doctor Name

Figure 2-36 New Doctor Name Added to Drop List of Doctors

FOR REFERENCE ONLY

8065751772 2.39
1.2 Procedure Type Button
The Procedure Type button in the Status Panel displays the currently-selected surgical
procedure name for the currently-selected doctor name. When pressed, this button
displays a drop list of the available procedures, named Procedure 1, Procedure 2,
etc. (see Figure 2-37). When a procedure is selected, the drop list collapses and the
procedure is selected.

The bottom button in the list, Manage Procedures…, is available when a doctor
other than Alcon Settings is selected. When pressed, the system transitions to the
Setup screen and opens the Manage Procedures dialog (see Figure 2-38). If there are
unsaved changes to the current procedure, a dialog to save or discard the changes is
presented, or the user can cancel the operation (X). The Manage Procedures dialog
allows the user to adjust the following:

Copy Procedure - Pressing this button opens the Procedure Names dialog to select a
new procedure name (see Figure 2-39). When a new procedure name is selected, the
new procedure is highlighted and it becomes the currently-selected procedure (see
Figure 2-40).

Delete Procedure - Selecting a procedure and pressing this button causes a

confirmation dialog to appear, allowing the user to delete the procedure. After
confirmation () the next procedure is highlighted.

Edit Procedure Comments- The Edit Procedure Comments dialog appears, along
with an alpha-numeric keypad, allowing the user to modify the comments under the
selected procedure name.

Import Procedure From Doctor - The Import Procedure dialog allows the user to
copy a doctor's procedure to a new doctor name. After confirmation, the last imported
procedure is highlighted, and that procedure becomes the currently-selected procedure.

Rename Procedure - Opens the Procedure Names dialog so the user can select another
name from the list.

Figure 2-37 Procedure Type Droplist

2.40
FOR REFERENCE ONLY 8065751772
 Figure 2-38 Manage Procedures Dialog

Figure 2-39 Procedure Names Dialog

Figure 2-40 Manage Procedures Dialog

FOR REFERENCE ONLY

8065751772 2.41
1.3 Remote Control Button
Pressing the Remote Control button icon in the Status Panel displays the remote
control's six snap keys (A, B, C, D, E, and F) as an overlay on the current screen
(white letters in center of black buttons, see Figure 2-41). This feature shows the
user which buttons to press on the remote control to quickly navigate around the
screen. Pressing the button again dismisses the overlay. The overlay is automatically
dismissed after 60 seconds, upon a step change, or upon transition between the Setup
Screen and Surgery Screen.

Snap Button A

Snap Button B

Snap Button D

Snap Button C

Snap Button E
Snap Button F

Figure 2-41 Remote Control Snap Navigation Buttons in Continuous Phaco Mode.

1.4 Front Panel Button

The Front Panel Status icon button, at the top-center position in the Status Panel, is a
rendering of the front connector panel. If no FMS or handpiece is inserted, the front
panel image is just shown as a ghosted outline of itself. If a FMS or handpiece is
inserted, the Front Panel Status button becomes animated.

• The rectangular FMS icon is colored pink when unprimed, and it is green when
primed. A label above the FMS icon indicates the type of FMS inserted into the
fluidics module (Active FMS or Gravity FMS or Calibration), or it is blank if an
FMS is not present. The label is red if FMS is not primed, and green when primed.

• The three handpiece ports are plain when no handpiece is connected, and colored
when a handpiece is connected (see Table 2-3). The name of the connected
handpiece (Phaco, PhacoT, UltraChop, UltraChopT, AutoSert®, AutoSertT, Not
Used, Unknown, or blank if a handpiece is not present. AutoSert® not available
in Infiniti® handpiece port 3) is printed to the right of its associated port. The
handpiece name is printed red if the handpiece is not ready for use (not tested) and
green when ready.
Port Color Name Color Indication
Plain No name No handpiece
Yellow Red Handpiece connected & selected, but not filled/tested
Yellow Green Handpiece connected & selected, and is filled/tested
Green Green Handpiece connected, not selected, and is filled/tested

Table 2-3 Status of Handpiece Connectors

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1.5 Footswitch Button
The Footswitch button icon depicts the type of footswitch connected to the Centurion®
Vision System (Centurion®, Centurion® Wired, or Constellation®). When button icon is
pressed, the Custom/Doctor Settings/Footswitch tab dialog appears (see Figure 2-46).

The side switches on the footswitch button icon become animated, and the system
emits a tone, when a switch is activated. Numbers on the footswitch's footpedal
Centurion®

reflect the position of the footpedal (0, 1, 2, 3) as it is being depressed and released.

The two paragraphs below apply to the Centurion® wireless footswitch, and do not
apply to the Centurion® wired or Constellation® footswitches.
Centurion® Wired

• A Footswitch Battery Status vertical bar, next to the Footswitch button, displays
the wireless footswitch's battery charge with three cells. If the charge is low, one
or two yellow cells are displayed; if charged, three green cells are displayed. The
battery status bar is always displayed in the Setup screen. If the footswitch is not
Constellation®
charging, and the battery charge is good, no icon is shown in the Surgery screen. If
the footswitch is not charging, and the battery charge is low, the bar blinks slowly in
both screens. If the footswitch is charging, the bar turns green with a lightning bolt
in the middle, and is shown in both screens.

• A stairstep bar-graph, located next to the Footswitch button, indicates the

Footswitch Signal Strength. If the wireless signal strength is low it shows 1 red
or 2 yellow bars; if signal strength is good it shows 3 to 5 green bars. If a wired
footswitch is being used, nothing is displayed. The signal strength icon is always
displayed in the Setup screen, but in the Surgery screen only when it is low.

1.6 Cumulative Dissipated Energy (CDE)

The current CDE value is displayed on this button. The Metrics dialog appears when
the button is pressed (see Figure 2-42). Metrics for Ultrasonics and Fluidics are
displayed for the current surgical procedure. Pressing the Cancel (X) button retains the
metrics and returns the system to the last screen used. Pressing the Reset Metrics ()
button resets all metrics to zero and returns the system to the last screen used.

The CDE values are reached using the equations shown in Table 2-4.

1.7 SGS Pairing Indicator

A ring of dots at the right end of the status panel indicates the status of the Surgical
Guidance System. A ring of dots indicates that the SGS is paired with the Centurion®
system, while no ring of dots indicates that the SGS is not paired. Pairing is
conducted in the Custom/System Settings/General window.

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 Figure 2-42 Metrics Dialog with Cumulative Dissipated Energy (CDE).

Total Case Time

The timer starts (Case Begin) when first step is chosen and footpedal is depressed. The timer stops (Case Ended)
when the FMS and all active handpieces are removed. The timer pauses when system is placed in Set-up mode
(Case is Inactive).

Ultrasonics
U/S Total Time: Sum of Longitudinal Time and Torsional Time.
Average Longitudinal Power: Average Longitudinal power over the time when Longitudinal power was applied.
For example, if Ultrasound Burst mode was selected and 100 mS burst pulses at 70% stroke were generated once
a second, the Average Longitudinal Power would record 70%.
Average Longitudinal Power (FP3): Average Longitudinal power over the time when Longitudinal power was applied
in footpedal position 3. This takes into account the U/S modulation aspects, resulting in a significantly lower reading
than Average Longitudinal Power. For example, if Ultrasound Burst mode was selected and 100 mS burst pulses at
70% stroke were generated once a second, the Average Longitudinal Power in Position 3 would record 7%.
Total Longitudinal Power On Time: Total time Longitudinal power was active. This records the Longitudinal On-
time, displayed in minutes and seconds.
Average Torsional Amplitude: Average torsional amplitude over the time when torsional power was applied. For
example, if OZil® Burst mode was selected and 100 mS burst pulses at 70% amplitude were generated once a
second, the Average torsional amplitude would record 70%.
Average Torsional Amplitude (FP3): Average torsional amplitude over the time when torsional power was applied
in footpedal position 3. This takes into account the U/S modulation aspects, resulting in a significantly lower reading
than Average Torsional Amplitude. For example, if Ultrasound Burst mode was selected and 100 mS burst pulses
at 70% amplitude were generated once a second, the Average Torsional Amplitude in Position 3 would record 7%.
Total Torsional Amplitude On Time: Total time torsional power was active. This records the torsional On-time in
minutes and seconds.
Equivalent Average Torsional Amplitude (FP3): Average U/S energy in footpedal position 3 calculated as:
0.4 x Average Torsional Amplitude in Position 3.
Equivalent Average Ultrasonic Power (FP3): CDE
U/S Total Time
Cumulative Dissipated Energy (CDE): Total U/S energy in footpedal position 3 (both longitudinal and torsional)
calculated as:
(Longitudinal Time x Average Longitudinal Power) + (Torsional Time x 0.4 x Average Torsional Amplitude)
The factor 0.4 represents approximate reduction of heat dissipated at incision as compared to conventional phaco.

Fluidics
Total Aspiration Time: Total time the system was aspirating.
Estimated Fluid Usage: An estimation of the volume of fluid aspirated based on system settings and time.

Table 2-4 CUMULATIVE DISSIPATED ENERGY (CDE) - CDE values are reached using formulas above.

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2. Setup Status Window
The Setup Status Window is where the current setup is displayed using images of the
Centurion® system with its attached accessories (see Figure 2-43), and is for display
only. This area also uses animated pictures to help the user perform procedures (i.e.,
luers being connected to a handpiece).

The system's setup status is displayed here through the use of pictures and text
messages. The user is alerted to situations like handpiece status, prime status, and
setup prompts.

A fluidics source must be installed: a bag of fluid in the bag bay for Active Fluidics™
technology, or a container of fluid hanging from the IV pole for Gravity Fluidics. The
type of fluidics chosen is shown on the left side of the screen.

If a valid FMS is not inserted, the user is asked to insert an FMS. When a valid FMS
is inserted, the fluidics mechanism performs a test of the aspiration pressure sensor. If
the test fails, a dialog is displayed and the FMS is rejected.

As each handpiece is connected to the system, it is shown on the screen. Its fill/test
status is represented through messages and color of the handpiece.

Custom Button
2. Setup Status Window

Figure 2-43 The Setup Status Window - In this image the phaco handpiece is filled and
tested and ready for surgery. Active Fluidics™ technology is being used as indicated
by the fluid bag on the left of the screen. If chosen as the preferred system of irrigation,
gravity fluidics is represented with a hanging bottle of fluid instead of the bag.

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 Custom Button
The Custom button, located half way up the right side of the Setup and Surgery
screens, enables the user to view and modify system settings, doctor settings, and
some surgical settings. When the Custom button is pressed, a drop list menu appears
with several available options (see Figure 2-44). When one of the options is selected
from the menu, the respective dialog for that option is displayed and the drop list
menu disappears. If no selection is made, the drop list menu disappears after about
five seconds.

The following describes the purpose of each drop list menu item, the function of
the controls in its dialog, and how the selections are invoked. The selections may be
invoked whether the footswitch treadle and/or a footswitch button is depressed or not
depressed, and the footswitch is functional when the dialog is displayed. The drop
list menu items provide the user with options relating to viewing, copying, deleting,
modifying, backing up, and restoring doctor/system settings.

• Doctor Settings
• Save
• Save As
• System Settings
• Backup / Restore
• Procedure Builder
• About
• View Events
• Shutdown System

Custom Button

Figure 2-44 Setup Screen with Custom Drop List Menu

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2.1 Custom / Doctor Settings
The Doctor Settings dialog is invoked when the user presses Doctor Settings on the
Custom drop list menu (see Figure 2-45). The Doctor Settings dialog enables the
user to view and modify surgeon preferences for the currently-selected doctor. The
first screen to appear contains settings in the General tab. Other tab settings are for
Fluidics, Footswitch, Sounds, SGS, and Advanced.

Each dialog has Confirm () and Cancel (X) buttons at the bottom of the screen.
When Confirm is selected, all settings changed since the dialog was invoked are saved
to persistent storage, the doctor dialog closes, and the settings take immediate effect.
If the current doctor is the Alcon Settings default, the changes take immediate effect,
but they are not saved to persistent storage; the changes are temporary. If Cancel is
selected, the whole doctor dialog closes and the system returns to its prior settings.

Figure 2-45 Doctor Settings Dialog Screen - General Tab

Custom / Doctor Settings / General Tab

• Default PEL (cm) - The (Patient Eye Level) adjustment is used to establish the
default PEL system offset for a particular surgeon. This is the value of PEL which
will be used for the selected surgeon unless the value is changed through the
Verify PEL function during system setup (see next description).

• Verify PEL (cm) - The Verify PEL button is used to automatically turn the Verify
PEL dialog On or Off. When turned On, the Verify PEL dialog is automatically
opened following the handpiece test. Upon completion of PEL verification, the
Surgery screen is automatically entered. When turned Off, the PEL step button at the
bottom of the Setup screen must be manually pressed to open the Verify PEL dialog.

• Default Procedure - Press this button to display a list of procedures the doctor can
select from to be his default procedure when beginning a case.

• Vit Setup - If the On button is selected, when entering the anterior vitrectomy
mode a window appears to guide the user through the Vitrectomy Setup.

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 Figure 2-46 Doctor Settings Dialog Screen - Fluidics Tab

Custom / Doctor Settings / Fluidics Tab

• Continuous Irrigation Auto-Off Threshold - The Continuous Irrigation Auto-Off
feature is used to automatically turn continuous irrigation Off when the handpiece
is removed from the eye. The threshold value ranges from 0 (Off) to 10 (Max).
The threshold is used to customize the performance to the particular surgical
environment such as tip/sleeve combination and height of instrument tray.

• Continuous Irrigation - Continuous Irrigation is applicable for lens removal, I/A,

and vitrectomy surgical steps. When Continuous Irrigation is set to On (enabled),
continuous irrigation will be active following the first footpedal depression and
the continuous irrigation On tone is generated. When transitioning to another
step of the same surgical type, continuous irrigation remains activated. When
transitioning to a step that is a different surgical type, continuous irrigation is
deactivated but then re-activated when the footpedal is depressed (except for
Coagulation and AutoSert®).

• Reflux Offset (cmH2O [hPa]) - Reflux pressure is limited to a level equal to the
current infusion pressure plus the value specified for the Reflux Offset, or the
maximum infusion pressure the system is capable of, whichever is less.

• Estimated Leakage Comp (cc/min [mL/min]) - Estimated Leakage Compensation

adjusts for pressure losses due to incision leakage while the system is maintaining
the programmed target IOP. Increasing this value is similar to adjusting the target
IOP setting.

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 • Irrigation Pressure Drop (%) - When the acquired value of the irrigation pressure
sensor is below the value specified by the Infusion Pressure Drop, the system will
display an advisory dialog. When this setting is 100%, this feature is disabled.

• Vent Time Adjustment - This feature is used to adjust the degree of venting
pressure at the handpiece tip that is adjusted in response to a vent (during
transition from footpedal position 2 to position 1). There are three settings: Min,
Medium, and Max. Minimum is the default which provides unmodified venting
performance. Settings Mid and Max increase the net pressure experienced at the
handpiece tip after a vent.

Figure 2-47 Doctor Settings Dialog Screen - Footswitch Tab

Custom / Doctor Settings / Footswitch Tab

• Button Assignment - Pressing a button next to a switch activates a drop-down list
with functions that can be selected for that footswitch button.
• Vit Cutter Button Dual Assignment - When in Anterior Vitrectomy mode of
operation, a selected footpedal button can be assigned the function of enabling
and disabling the vitrectomy cutter function. This button, when in other modes,
has a different assignment.
• Footswitch Range Spans (%) - The buttons on the screen allow you to adjust the
treadle settings to your own personal preferences.
• Detent - The user can set the amount of Strength required to transition through the
footpedal detents, and the footpedal Vibration feature can be turned On or Off.

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 Figure 2-48 Doctor Settings Dialog Screen - Sounds Tab

Custom / Doctor Settings / Sounds Tab

The Sounds to Adjust dialog enables the surgeon to set a volume level for all tones
and voice confirmations. The volume levels are set individually or all at the same time
by pressing the Individual or All button at the top of the screen. When an individual
button is selected, the volume level adjustment will pertain only to that selection.
The tones and voices are adjusted with the Volume buttons located at the bottom of
the screen. Each selection – except for Vacuum Level, Phaco Occlusion, Coagulation
Power, and Low Bag Fluid Voice – may be turned Off so that no tone will be heard.
Pressing the Play button emits a sample of the volume level selected.

Figure 2-49 Doctor Settings Dialog Screen - SGS Tab

Custom / Doctor Settings / SGS Tab

For details on the features associated with the optional Surgical Guidance System,
refer to your SGS operator's manual addendum.

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 Figure 2-50 Doctor Settings Dialog Screen - Advanced Tab

Custom / Doctor Settings / Advanced Tab

• AutoSert® Full Extension Offset (mm) - When using a D/C cartridge, this feature is
used to adjust the full extension position at which the AutoSert® IOL injector stops
moving forward. The adjusted position is defined in millimeters relative to the
maximum extension position. At the default setting (0) the AutoSert® IOL injector
is at its maximum extension.
• AutoSert® Remote Default - When using a D/C cartridge, the Load Plunger and
Preload IOL buttons are selected to set the default value of the remote control
focus to be either Load Plunger or PreLoad IOL buttons.
• Irrigation Tone - Pressing the Irrigation Tone On or Off button determines
whether or not the current doctor's preference is to hear a clicking sound as the
footpedal is depressed and fluidics begin flowing, and again when the footpedal is
released and fluidics stop.
• CME Compliant Video Overlay - If the system is connected to a CME (Continuing
Medical Education) Compliant Video Overlay, the On button should be selected;
if not, select the Off button. This feature causes the Alcon logo to be displayed or
not displayed on the VideOverlay.

8065751772 2.51
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2.2 Custom / Save
The Save dialog can be invoked when a change has been made to the current surgical
parameters and the user selects the Save option from the Custom drop list menu (see
Figure 2-43). If there are no unsaved changes, or if no active surgery has taken place,
the Save button is disabled.

The Save dialog provides the user with Save () and Cancel (X) buttons. If the Save
Changes button is pressed, the changes are saved to the current doctor. If Cancel is
selected, surgical parameters are not saved and the dialog closes.

The Alcon Settings doctor is the factory default and cannot be permanently changed,
so the Save button is disabled when Alcon Settings is the current doctor.

2.3 Custom / Save As

Pressing the Save As button (see Figure 2-43) opens the Enter Doctor Name dialog for
creation of a new doctor as a copy of the active doctor settings. A keyboard appears
on the screen allowing the user to type a new doctor name. Adding a new doctor does
not change the currently-selected doctor. If the maximum number of doctors has been
reached, a notification dialog appears.

Figure 2-51 Save As Dialog Screen

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2.4 Custom / System Settings
The System Settings dialog only opens when in the Setup Screen. If in an inactive
Surgery Screen, the system transitions to the Setup Screen and the System Settings
dialog opens. If a surgical case is active, a confirmation dialog opens stating that
the Setup Screen must be entered before proceeding, requiring confirmation before
transitioning to the Setup Screen/System Settings dialog.

Custom / System Settings / General Tab

• Irrigation Type Default - This button sets the type of fluidics displayed as the
system default. The Active Fluidics™ FMS is shown with a bag of BSS® irrigating
fluid in the system's bag bay. The Gravity fluidics FMS is shown with a container
of BSS® irrigating fluid hanging from the IV pole hook.

• Irrigation Fill - When Irrigation Fill is turned On, irrigation is activated without
reflux to the handpiece (fluid will only stream from irrigation port). The result is
that the Irrigation Fill step replaces the Fill step, in all instances, for all users of the
console. When turned Off, the Fill step activates both irrigation and reflux to clear
air bubbles from the fluidics system.

• Date and Time - Pressing the Change Date and Time button allows the user to
change the date and time.

• Remote Control - Pressing the Change Remote Control button allows the user to
change the remote control communication channel in the event of a conflict with
another system.

• Language - Pressing this button presents a list of available languages to be used

by all users of the system.

Figure 2-52 System Settings Dialog Screen - General Tab

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 • System Name - Pressing the Change System Name button brings up a keyboard so
the user can change the system name to facilitate identification.

• SGS Pairing - To change pairing of the Surgical Guidance System, press Change
SGS Pairing to bring up its dialog. Press Find, and after the SGS device is located,
the SGS ID number is displayed. Select the desired SGS device, then press the
Pair button. The device ID number of the Paired SGS device will be displayed.

• SI Units - Display objects are converted to SI units when turned On. The unit
labels and displayed values are converted as follows:

Default Units Label SI Units Label SI Value

“mmHg” “hPa” hPa = mmHg * 1.33322
“cmH2O” “hPa” hPa = cmH2O * 0.980638
“cc/min” “mm3/sec” mm3/sec = cc/min * 16.667

Note that Equivalent Bottle Height is an alternate representation of the IOP

surgical parameter. It is not itself a setting or actual value, and is never displayed
in SI units.

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 Custom / System Settings / Wireless Tab
• Footswitch Network - This setting is used to turn the wireless footswitch network
on or off. When the wireless network is OFF, an icon appears in the status panel
below the CDE display indicating that the wireless connection has been disabled.

• Footswitch Channel - Used to adjust the displayed channel value up or down,

allowing user to select different frequency bands such that signal integrity can be
maximized. For an indication of wireless channel integrity, a Green circle indicates
high quality, yellow medium quality, amber low quality, and red indicates the
signal is too weak to use. May be invisible for up to 10 seconds after Wireless tab is
selected. If Footswitch Network setting is changed from Off to On, the Footswitch
Channel Quality Status will not become visible until changes are saved.

• Footswitch Network Region - This feature establishes the appropriate network

configuration for the particular region of the world (Japan, North America, World).
To change the wireless channel for the footswitch, the footswitch must first be
cradled onto the back of the system. This "pairs" the footswitch with the system and
allows the wireless channel to be changed. Note that since the wireless footswitch
and the Surgical Guidance System (SGS) device share the same network, changing
the wireless channel for the footswitch requires a re-pairing of the SGS device by
depressing the Change SGS Pairing button under the General tab.

• Wi-Fi Network - These buttons turn the Wireless Footswitch/Surgical Guidance

System wireless network On and Off. If it is desired to use the SGS or footswitch
wirelessly, then the wireless network must be turned ON.

• Wi-Fi Channel - Sets wireless channel. Change this setting in the event of a conflict
with another wireless device. See Footswitch Channel for wireless channel integrity.

• Wi-Fi Network Region - The Wi-Fi Network Region setting (Europe, Japan, North
America) matches the system to its geographic location. This establishes the
appropriate network configuration for the particular region of the world.

• Wi-Fi SSID - Shows Current Wi-Fi Network SSID system setting; this is the
unique identification of the system on the Wi-Fi network. The Change SSID
button is used to modify the system identification on the network.

Figure 2-53 System Settings Dialog Screen - Wireless Tab

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 Figure 2-54 Backup/Restore Dialog Screen - Backup Tab

2.5 Custom / Backup/Restore / Backup Tab

This dialog contains a list of all doctors on the system, except Alcon Settings. When
a selected doctor name is highlighted, the Backup Doctor button is enabled. With
USB removable media (flash drive) inserted into the rear panel's USB slot, pressing
Backup Doctor copies the highlighted doctor file from the console to the flash drive.
With no doctor name highlighted, pressing the Backup All Doctors button copies the
full backup (all doctor files except Alcon Settings) from the console to the flash drive.

Figure 2-55 Backup/Restore Dialog Screen - Restore Tab

Custom / Backup/Restore / Restore Tab

With USB removable media (flash drive) inserted into the rear panel's USB slot, this
dialog contains a list of all doctors on the removable media. When a selected doctor
name is highlighted, the Restore Doctor button is enabled and can be pressed to copy
the doctor settings to the console. With no doctors highlighted on the flash drive, the
Restore All Doctors button is enabled, allowing the system to perform a full backup
from the highlighted directory on the flash drive to the console. If a doctor file already
exists, the Resolve Name Conflict dialog appears and must be resolved.
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2.6 Custom / Procedure Builder
The current doctor can customize his surgery steps across the bottom of the surgery
screen by using the Procedure Builder dialog (see Figure 2-56). Steps can be added,
deleted, copied, and renamed; and the sequence of steps can be reordered with the
Move buttons.

The Procedure Builder dialog only opens in the Setup Screen. If the user is in an
inactive Surgery Screen, the system transitions to the Setup Screen and the Procedure
Builder dialog opens; if a surgical case is active, the Return to Setup confirmation
dialog opens, requiring user confirmation before transitioning to the Setup Screen/
Procedure Builder dialog.

Pressing the New Step button in the Procedure Builder dialog opens another dialog
that offers all available steps that can be selected (see Figure 2-57). Selecting a step
closes that dialog and places the step at the bottom of the Procedure Builder dialog
where it can be moved up to the user's desired position.

Selecting a step in the Procedure Builder dialog allows the user to move the step up or
down, or to delete the step completely.

Figure 2-56 Procedure Builder Dialog - When Procedure Builder is selected from the
Custom drop down list, the Procedure Builder dialog appears. All the steps for the
currently-selected doctor/procedure are shown from top to bottom. Pressing the New
Step button brings up a dialog with available steps that can be added to the procedure.

8065751772 2.57
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 Figure 2-57 Procedure Builder Dialog with Available Steps - Pressing the New Step
button causes a dialog to appear with available steps that can be added to the selected
doctor's procedure.

Figure 2-58 Procedure Builder Dialog with Fill Step Added - In this case the Fill step
was selected from the right column of the Steps dialog (see prior figure). The Fill step
appeared at the bottom of the existing steps, then the Move Up button was pressed to
place the Fill step after the Epi step. More steps can be added, deleted, or moved prior
to saving the action by pressing the Confirm () button.

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 Figure 2-59 Step Selected in Procedure Builder Dialog - Selecting a step in the Proce-
dure Builder Dialog allows the user to Delete, Copy, Rename, or Move the step.

Figure 2-60 Copy (or Rename) Step in Procedure Builder Dialog - In this case, the
user selected Copy Step from the Procedure Builder Dialog, although Rename step
brings up the same selections for the type of step selected. Copying a step duplicates
all the doctor's settings to the new step name, while renaming a step simply changes
the name of the step.

FOR REFERENCE ONLY

8065751772 2.59
 Figure 2-61 The About Dialog - Upon installation by an Alcon service technician, a
phone number for local technical assistance is programmed into the system and is
displayed the bottom of the dialog (not shown in this image).

2.7 Custom / About

For a quick reference to the Centurion® system's configuration, open the Custom /
About dialog. It is here you will find versions of Software, Hardware, and Logicware
for system components (Host, I/A, Generator, MultiFunction, Footswitch) .
Also shown are the versions of the Console and Footswitch Modems, and of the
Footswitch Battery. Pressing the Patents button brings up a dialog of the Centurion®
System's patent numbers. A phone number for technical assistance is printed at the
bottom of the About dialog.

Figure 2-62 The Event Viewer Dialog.

2.8 Custom / View Events

This dialog contains information important to the service technician. The user can
select an Event in the upper dialog to read its Event Detail below.

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 Figure 2-63 The Shutdown System Dialog.

2.9 Custom / Shutdown System

Pressing this button displays the Shut down the system? confirmation dialog. If
canceled (X), the system will not shut down. If confirmed () the I/V pole lowers to
its bottom position and the console shuts down.

8065751772 2.61
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3. Setup Steps
This area of the Setup Window is used for initiating setup functions (see Figure 2-64).
If a user-defined doctor has been added in addition to Alcon Settings, at power-up the
system enters the grayed-out Setup Screen with the Select Doctor dialog displayed.
In this case, one of the doctor names must be selected to continue with the system
setup. After selecting a doctor, the Setup Screen appears, and the Prime FMS button is
highlighted.

PRECAUTION: It is important to follow the setup sequence as indicated on the

Centurion® Vision System display screen and/or as written in section three of this
operator's manual. Not following the directions could lead to priming failures.

Prime FMS / Prime Bag Button

When the system is initially turned on, the button is labeled Prime FMS. After
priming, for Active Fluidics™ technology the button becomes Prime Bag, but for
Gravity Fluidics the button remains Prime FMS. The Prime FMS / Prime Bag button
may be selected as long as a valid fluid container and FMS is installed, regardless of
current prime and tune status.

With the irrigation and aspiration luer fittings connected together, the priming
sequence can be initiated. When selected, a Prime FMS or Prime Bag dialog appears
with a progress bar that shows the progress of the draw fluid priming sequence. When
the priming and vacuum checks are completed successfully, the prime status becomes
“Primed” and the Fill Button is highlighted.

Fill Button
The Fill button is automatically highlighted when the priming sequence has
completed successfully. With handpiece inserted, and irrigation / aspiration tubing

3. Setup Steps
Surgery Button
PEL Button
Test Handpiece Button
Fill Button
Prime FMS / Prime Bag Button

Figure 2-64 The Setup Steps Window

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 connected to it, pressing the Fill button activates the fluidics system to fill the
handpiece. During the fill process the Fill Handpiece dialog appears on the screen
with a progress bar that shows the progress of the filling sequence. Also displayed in
the dialog is a Cancel button (X) and an Advance to Test Handpiece button.

Once the fill sequence is initiated it can be aborted by pressing the Cancel button (X),
whereby the Fill Handpiece dialog closes and the Fill button darkens but remains
highlighted. If Advance to Test Handpiece is pressed, the Fill dialog closes and the
Test Handpiece function is selected.

Test Handpiece Button

The Test Handpiece button may be selected only when the FMS is primed and a
phaco handpiece is connected.

The Centurion® Vision System allows a CENTURION® OZil® handpiece and

INFINITI® OZil® handpiece to be connected at the same time, but the user must
perform the Test Handpiece sequence for each handpiece. Pressing the Swap Phaco /
UltraChop button switches handpieces for the testing sequence.

When the Test Handpiece button is selected the test handpiece dialog will display
progress of the flow check and vacuum check. A Cancel button also appears. Once the
test sequence is initiated, it can be aborted by the user by pressing the Cancel button
(X) or removing the FMS, or it can be left to proceed to completion.

PEL Button
By default, the Verify PEL (cm) dialog appears upon successful completion of the
handpiece test sequence. This can be changed to a manual step by entering the
Custom/Doctor Settings/General dialog and pressing the Verify PEL Off button.

Test ICD Button

The Test ICD button may be selected only when a single-use INTREPID®
Capsulotomy Device (ICD) handpiece has been connected, and the current doctor
has added the Capsulotomy step through the Custom / Procedure Builder feature. The
color of the ICD image indicates its ready state: red for not ready (not tested or failed
test), or green for ready (successfully tested).

When connected, the Test ICD button replaces the Test Handpiece button used with the
phaco handpiece. The Test ICD button must be pressed to prepare it for a capsulotomy.

The ICD must be enabled upon entering the Capsulotomy step, but if the ICD has
not yet been tested, the user will be asked to go back to the Setup screen for testing.
Pressing the Enable button in the Capsulotomy step screen is the last preparatory step
prior to performing the capsulotomy. In this step, the Reflux switch can also be used to
enable the the ICD.

Surgery Button
If the Surgery button is pressed the system goes to the appropriate Surgery Screen as
determined by the procedure selected. The first surgery step for the doctor’s procedure
is entered.

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SURGERY SCREEN AND ITS FUNCTIONS

The Surgery Screen contains the buttons, readouts, and controls that allow the user to
perform surgical functions. This screen is displayed when one of the following occurs:
• The Surgery button is pressed from the Setup Screen.
• The handpiece and priming functions are completed in the Setup Screen and no
other connected handpieces are “Not Tuned.”

The Surgery Screen is divided into three sections (see Figure 2-65). At the top is the
Status Panel, below that is the Surgery Window, and below that is a row of Surgery
Steps.

Depending on the procedure type and surgery step selected, the Surgery Screen
contains tools and surgical parameters corresponding to the selections. Although
several representative surgery screens are shown in this section of the manual, not all
screens showing handpiece/procedure/steps are shown.

1. Status Panel
The buttons in the surgery Status Panel are the same as the buttons in the setup Status
Panel (see Setup Screen earlier in this section of the manual for descriptions).

2. Surgery Window
The Surgery Window occupies the center of the Surgery Screen and is broken into
upper and lower halves. The top half has the surgery controls, and the lower half has
the fluidics controls, both of which are described on the following pages.

The actual values for certain parameters are shown in oval display buttons. With
the exception of the Vacuum parameter, the upper limit for each setting represents

1. Status Panel
(descriptions are the same
as in the Setup Screen)

2. Surgery Window

3. Surgery Steps

Figure 2-65 The Centurion® Vision System Surgery Screen - This screen is for phaco
modes of operation. The screens for other modes of operation look similar to this, but
may have more or fewer oval display buttons and surgical parameters corresponding to
the surgery step.

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 its maximum setting. (For the Vacuum limit setting, if the vacuum limit is set to
700+ mmHg [933+ hPa], then the upper limit does not exist.)

Each surgery step has operating parameter settings that are established by default.
During surgery the user may change the parameters in any of the steps. Any
parameter changes made may be explicitly saved by the user using the Save As
option (if Alcon Settings is doctor) or the Save option (if other than Alcon Settings is
doctor) from the Custom drop list. Also, if there are unsaved changes to the surgery
steps and the user changes the doctor or lens removal procedure, a dialog box appears
asking the user to save or discard any unsaved changes. Powering down the system
automatically dismisses any unsaved changes.

2.1 Surgery Controls

For Phaco steps, Coag steps, Vitrectomy steps, Coagulation steps, and AutoSert®
injector steps, the upper half of the Surgery Window contains the surgery controls (see
Figure 2-66). The surgery controls available are dependent on the type of step selected.

Mode Button
The Mode button in the top-center of the Surgery Controls area displays the current
mode for the step; in Figure 2-66 it is Continuous mode in the PrePhaco step. The
Phaco and Anterior Vitrectomy modes can be changed by pressing the top-center
Mode button and selecting another from a drop list. Depending on the current step,
the Alcon Settings mode selections are:

Phaco Irrigation/Aspiration AutoSert® Coagulation Anterior Vitrectomy

• Continuous • Irr / Asp • AutoSert® • Coagulation • Anterior Vit
• Pulse • Epi Removal
• Burst • I/A Cut
• Peripheral Irid
• Visco Asp

Mode Button IP (Intelligent Phaco) Button

Status Panel

2.1 Surgery Controls Oval Display Buttons

Custom Button

Task Light Button

Fluidics Controls

Surgery Steps

Figure 2-66 Surgery Control Window with Phaco Surgery Controls Identified - This upper
half of the Surgery Control Window is used to observe current surgical performance levels,
and to adjust surgery settings by pressing the oval display buttons and buttons to present
control dialogs.

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 Oval Display Buttons
Oval display buttons (see Figure 2-66) show parameter settings for a procedure in
its current step. Pressing an Oval Display Button brings up a dialog where the user
can change settings for each footpedal position within a step (see Figure 2-67). This
dialog includes buttons to toggle between linear (/) or fixed (–) footpedal control, up
and down buttons to adjust setting values in small increments, and slide buttons to
quickly adjust setting values in large increments.

Press this button to toggle between linear (/) or

fixed (–) footpedal control of surgical parameters
For torsional amplitude, 0% is the setting
when footpedal enters position 3, and 20%
is the upper limit setting when footpedal
is fully depressed.

Up and Down buttons are used to

make incremental adjustments to
torsional amplitude.

Slide button is used to quickly

make large adjustments to
torsional amplitude.

This adjustment dialog is for This oval display window is a visual representation of
footpedal position 3 torsional amplitude from left to right through footpedal position 3.

Figure 2-67 Oval Display Button Dialog - Oval display buttons on a surgical screen show
parameter settings for a current step (see Figure 2-66). Pressing an oval display button
brings up a dialog where the user can make adjustments to the settings according to
doctor's preferences.

Task Light Button

This button is pressed to turn the front panel task light on and off. When turned on the
icon in the Task Light button shows light rays; when turned off the light rays are muted.

Custom Button
Pressing this button presents a list of features that can be selected, allowing the user
to adjust system settings to the surgeon's preferences. This feature is discussed at
length earlier in this section of the operator's manual.

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 IP Button
Intelligent Phaco (IP) is used to deliver a reduced magnitude of phaco energy when
a vacuum threshold setting is exceeded. This reduced phaco energy is applied only
as necessary, and continues until the vacuum drops below the trigger threshold. The
same IP settings are used for each enabled phaco step.

Pressing the IP button while in a phaco step causes the IP Settings dialog to appear
on the screen (see Figure 2-68). Intelligent Phaco is enabled by pressing the On
button, or disabled by pressing the Off button. After selecting On or Off and pressing
the confirmation button (), the dialog closes. When the IP feature is enabled for a
particular phaco step, the IP button is animated; when disabled, it is colored gray.

The adjustable settings are Longitudinal Pulse Duration, Vacuum Threshold, and
Longitudinal/Torsional Ratio. These settings are user-adjustable so the user can
specify the vacuum limit at which the IP feature is activated, and the amount of
energy that is delivered when activated.

• Longitudinal Pulse Duration (ms) - Longitudinal Pulse Duration specifies the on-
time of an applied longitudinal phaco pulse during activation, from 0 to 20 pulses
per millisecond. These phaco pulses are applied until the vacuum level falls below
the Vacuum Threshold setting.

• Vacuum Threshold (% of Vacuum Limit) - The Vacuum Threshold setting determines

the percentage of the vacuum limit set value at which the IP feature is activated and
its specified phaco power is applied. When vacuum reaches and/or exceeds the
vacuum threshold, then the IP feature, if enabled, is activated. When the vacuum
drops below the vacuum threshold value, then the IP feature is deactivated. The
vacuum threshold ranges from 90% to 100% of vacuum limit.

• Longitudinal / Torsional Ratio - The Longitudinal / Torsional Ratio establishes the

applied phaco power level relative to the applied torsional amplitude. This ratio is
expressed as a decimal fraction and ranges from 0.5 to 1.0.

Figure 2-68 IP Dialog - Intelligent Phaco can be turned on and off for the current step by
pressing the On and Off buttons in this dialog, then pressing the confirmation button ().

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2.2 Fluidics Controls
The lower half of the Surgery Window contains the Fluidics Controls (see Figures
2-69 and 2-70). These parameters always involve irrigation, vacuum, and aspiration
controls, and are independent of the Surgery Controls. Fluidics Controls are available
in all steps but AutoSert® and Coagulation.

Fluidics Administration
The Centurion® Vision system supports two types of fluidics administration to deliver
and control fluid pressure: Active Fluidics™ technology is an automated system that
administers fluid from a bag of BSS® irrigating fluid within its bag bay (see Figure
2-69), and Gravity Fluidics is used for fluid administration using the power IV pole
(see Figure 2-70).

IOP Control (used with Active Fluidics™ technology)

When the Active Fluidics™ FMS is used, IOP (IntraOcular Pressure) control
functionality becomes enabled. Active Fluidics™ technology allows control and
maintenance of intraocular pressure under the varying conditions experienced during
surgery. Figures 2-71 (fixed) and 2-72 (linear) depict the surgery screen with Active
Fluidics™ technology in use. The vertical lines within the oval display button depict
the separation of footpedal positions.

IOP Fluid Bag (used with Active Fluidics™ technology)

The IOP fluid bag “fuel gauge” provides an estimated value of remaining BSS®
irrigating fluid within the irrigation bag when using the Active Fluidics™ FMS. As
the procedure progresses the indicated value ranges from full (>500 ml) to empty
(0 ml). If the volume drops to below 100 ml, the bag color changes from blue to red.
An advisory is issued when the usable bag volume drops to 0 ml.

IOP Settings (used with Active Fluidics™ technology)

Pressing the IOP oval display button brings up the IOP Setpoints dialog (see Figures
2-71 & 2-72). This dialog allows for tailoring of IOP level as a function of footswitch
position. The vertical separation lines indicate the transition point between footswitch
positions. The dialog in Figure 2-72 shows that linear/fixed buttons have been
pressed to activate fixed footpedal control in position 1, and linear footpedal control
in footpedal positions 2 and 3. The Up/Down buttons, or the Slide button, have been
used to adjust new IOP settings.

IV Pole Settings (used with gravity fluidics)

When the Gravity Fluidics FMS is used, traditional gravity-fed irrigation pressure is
provided from a container of BSS® irrigating fluid hung from a hook on the motorized
IV pole (see Figure 2-70). Irrigation pressure is increased or decreased by raising or
lowering the IV pole.

Using gravity fluidics, raising the IV pole to its maximum height of 150 cm results
in maximum irrigation pressure (150 cm includes a 110 cm maximum vertical height
above the pressure sensor plus a maximum PEL of -40 cm). In the event of power
loss, bottle position is maintained; however, if the unit is turned off using the Standby
switch, the IV pole automatically retracts to its storage position.

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 IOP Fluid Bag IOP Settings Vacuum Settings Aspiration Settings

Status Panel

Surgery Controls

2.2 Fluidics Controls

Surgery Steps

Continuous Irrigation PEL (cm) Flow Comp (x)

Eq. Bottle Height = (cmH2O) Vacuum Rise IOP Ramp (sec)

Figure 2-69 Fluidics Control Window with Active Fluidics™ Technology Selected - The lower half of the
Surgery Control Window is used to observe current fluidics performance levels, and to adjust settings
by pressing the oval windows and buttons to present control dialogs.

IV Pole Settings Vacuum Settings Aspiration Settings

Status Panel

Surgery Controls

2.2 Fluidics Controls

Surgery Steps

Continuous Irrigation PEL (cm)

Bottle Height (cmH2O) Vacuum Rise

Figure 2-70 Fluidics Control Window with Gravity Fluidics Selected - The lower half of the Surgery
Control Window is used to observe current fluidics performance levels, and to adjust gravity fluidics
settings by pressing the oval windows and buttons to present control dialogs.

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 Pressure is fixed throughout
footpedal positions 1, 2, and 3

Figure 2-71 IOP Setpoints (Fixed) for Active Fluidics™ Technology - Pressing the IOP (mmHg or hPa)
Oval Display Button brings up the IOP Setpoints (mmHg or hPa) dialog.

Pressure is fixed in Pressure rises linearly throughout

footpedal position 1 footpedal positions 2 and 3

Up Button

Slide Button

Down Button

Figure 2-72 IOP Setpoints (Linear) for Active Fluidics™ Technology - This IOP Setpoints dialog is an
example of how footpedal settings have been changed in linear and fixed manner in the
three footpedal ranges. The new settings are accepted by pressing the green confirmation
button (  ).

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 Vacuum Settings
The operator can adjust the vacuum limit (Vacuum / mmHg) using the front display
panel or the remote control. The adjustable vacuum limit range is 0 to 700+ mmHg (0
to 933+ hPa), where 700+ mmHg (933+ hPa) is limited by atmospheric pressure.

Aspiration Settings
The operator can adjust the aspiration limit (Asp Flow / cc/min) using the front
display panel or the remote control. The adjustable aspiration limit range is 12 to
60 cc/min (12 to 60 mL/min).

Continuous Irrigation
Continuous Irrigation (Cont Irr) is available in most surgical steps (except
Capsulotomy, AutoSert®, Coag) and allows for irrigation of the eye during surgery
by opening the irrigation valve, regardless of footswitch position. The Continuous
Irrigation mode default setting can be set to On or Off through the Custom / Doctor
Settings / Fluidics tab.

When Continuous Irrigation is enabled, footpedal range 1 is eliminated, thereby

expanding the range of footpedal position 2. Continuous Irrigation remains enabled
until transitioning to another step where Continuous Irrigation is disabled (irrigation
valve off). Continuous Irrigation may also be automatically turned off when the tip is
removed from the eye as determined by the Continuous Irrigation Auto-Off Threshold
setting (Custom / Doctor Settings / Fluidics tab).

Continuous Irrigation can be turned On and Off by doing the following:

- Press the Cont Irr button on the surgery screen.
- Use the remote control's Parameter Selection keys to select the Cont Irr button, then
press the + or - key on the remote control.
- Program a footswitch switch for the Continuous Irrigation function, then press the
designated switch on the footswitch.

PRECAUTION: Before switching handpieces it is advised to exit the eye, then turn
Continuous Irrigation off to close the irrigation valve and prevent excess BSS® sterile
irrigating solution from flowing out of the handpiece.

Eq. Bottle Height = (cmH2O) (used with Active Fluidics™ technology)

Equivalent Bottle Height is calculated when using Active Fluidics™ technology
to present the comparative bottle height if the IV pole was used for fluidic
administration. The equivalent IV pole height is calculated from the value in the IOP
oval display button (1 mmHg = 1.36 cmH20 = 1.33 hPa).

Bottle Height (cm) (used with gravity fluidics)

This readout shows the irrigation pressure at the selected IV pole height.

PEL (cm)
The PEL button allows adjustment of the Patient Eye Level setting from the surgery
screen. (For details on setting the PEL, see the Setup Screen description.)

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 Vacuum Rise
At the onset of an occlusion, it may be desired to slow down the activity at the
ultrasound tip. The Vacuum Rise feature slows the aspiration pump rate, decreasing
the rate at which vacuum level rises when the ultrasound tip begins occluding. The
setting values range from 0 (unadjusted rise time) to -1 to -2 (slowest rise time).

IOP Ramp (s) (used with Active Fluidics™ technology)

IOP Ramp control applies whenever Active Fluidics™ technology is used and the
IOP function is set to a fixed pressure level. It allows adjustment of the time it takes
to ramp up from no irrigation pressure to its preset fixed value when entering, and
traveling through, footpedal position 1; although, if the footpedal travels immediately
from position 0 to positions 2 or 3, the IOP goes instantly to its fixed IOP setting.
When the IOP Ramp button is depressed, an adjustment pop-up dialog is displayed
which allows adjustment of the transition time from 0 seconds (Fast) to 2.0 seconds.
The Anterior Vitrectomy IOP ramp setting is independent from phaco and I/A steps.

Irr Factor (x) (used with Active Fluidics™ technology)

When Active Fluidics™ technology is used, the Irrigation Factor (Irr Factor) function
is available, and works in conjunction with the Estimated Leakage Comp feature
(Custom/Doctor Settings/Fluidics). This feature attempts to compensate for the
pressure losses along the irrigation path by adding a factor which is based on the
estimated irrigation fluid flow. The scale factor ranges from Off (0) to 2; the larger the
value the more compensation is employed. This scale factor is empirically adjusted to
compensate for numerous factors including: tip, sleeve, wound architecture, wound
size, and surgical technique.

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2.3 Surgery Window with Phaco Steps
Surgery controls vary with the phaco step and mode currently selected, although all
phaco steps contain Longitudinal (%) and Torsional (%) settings. If the top-center
Mode button is pressed, Continuous, Pulse, and Burst modes are offered in a drop list
with different settings for each, as shown in the table below. All phaco steps contain
the same fluidics controls for irrigation, vacuum, and aspiration.

Adjustable Settings in Selected Phaco Mode

Continuous Longitudinal (%) Torsional (%)
Pulse Longitudinal (%) Time On (%) Pulse Rate (pps) Torsional (%) Time On (%)
Burst Longitudinal (%) On Time (ms) Off Time (ms) Torsional (%) On Time (ms)

Figure 2-73 Surgery Window with Phaco Steps

2.4 Surgery Window with I/A Steps

All I/A steps contain the same fluidics controls for irrigation, vacuum, and aspiration.
Surgery controls are not used with the Irr/Asp step; the surgery controls area only
displays the Mode button showing Irr/Asp. (Although, if AutoSert® injector step is
enabled while in an I/A step, the AutoSert® injector setup dialog is displayed in the
Surgery Controls area. See INTREPID® AutoSert® IOL Injector Setup for details.)

Figure 2-74 Surgery Window with I/A Steps

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2.5 Surgery Window with AutoSert® Injector Step
The AutoSert® injector step contains a dialog at the right side of the Surgery Controls
area to assist the user when setting up the INTREPID® AutoSert® IOL Injector. the
Surgery Controls area also has oval display buttons that are used to set the rate of IOL
lens insertion. Fluidics controls are not used with the AutoSert® injector step.

Figure 2-75 Surgery Window with AutoSert® Injector Step

2.6 Surgery Window with Coagulation Step

The Coagulation step contains just one surgical parameter: Power (%). This parameter
is displayed in the upper portion of the Surgery Controls window. This window also
contains a mode indicator showing Coagulation. Fluidics controls are not used with
the Coagulation step.

Figure 2-76 Surgery Window with Coagulation Step

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2.7 Surgery Window with Anterior Vitrectomy Step
The Vitrectomy step contains a surgery control for Cut Rate parameters, and fluidics
controls for irrigation, vacuum, and aspiration parameters. The Surgery Controls area
also contains a top-center Mode button indicating the current V itrectomy mode, of
which four are available (Anterior Vit, Epi Removal, Peripheral Irid, Visco Asp).

Figure 2-77 Surgery Window with Anterior Vitrectomy Step

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3. Surgery Steps
Surgery screens contain step buttons at the very bottom of the screen (see Figure
2-78). These buttons represent all the surgery steps for the currently-selected doctor,
plus a Setup button to quickly return to the Setup screen.

The row of Surgery Steps allows up to 12 visible buttons at one time across the
bottom of the surgery screen. The Setup button is always on the far left, and the Coag
& Ant Vit buttons are on the right for all surgical modes.

Procedural step buttons can be added or removed from a doctor's surgery steps by
selecting or removing them in the Custom / Procedure Builder dialog.

Nine visible procedural step buttons are located between the Setup button and the
Coag/Vit buttons; however, up to 16 procedural step buttons can be programmed into
this space by the current doctor. When more than 9 procedural steps are programmed,
and when selecting the step that is furthest left (next to the Setup button) or furthest
right (next to the Coag/Vit buttons), the steps will scroll so that all steps before or
after the selected step can be seen.

Status Panel

Surgery Controls

Fluidics Controls

3. Surgery Steps

Lens Removal Steps I/A Steps

Setup Button Coag Step Vit Step

Procedural Step Buttons Stationary Step Buttons

Figure 2-78 Surgery Steps - At the bottom of the Surgery Screen are the Surgery Steps.
The buttons in this area allow the surgeon to control the surgical step progression.

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3.1 Setup Button
When the Setup button is pressed, the user will be taken to the Setup screen. To enter
the Setup screen the footpedal must be released, and the footswitch buttons must not
be activated.

3.2 Procedural Step Buttons

When a surgery step is selected, its button expands in size and becomes animated,
and the surgical parameters for the surgery step are displayed in the Surgery Window.
Pressing Procedural Step Buttons is allowed regardless of footpedal position. A step
change into Coag or Vit is allowed with the footpedal depressed, but the footpedal
must be released to exit.

The Centurion® Vision System provides operational surgical steps to support efficient
lens removal and IOL implantation. Each step allows for the adjustment of surgical
parameters such as power, aspiration, and vacuum settings according to doctor
preferences. These step buttons are arranged in sequential order from left to right
across the bottom of the screen to provide a complete surgical procedure of different
settings associated with different aspects of the procedure.

Factory-preset operating parameters for each step are programmed into the system as
"Alcon Settings." These default operating parameters can be temporarily modified,
and then they can be permanently saved with a new doctor's name by using the
Custom / Save As dialog.

The procedural steps are selectable from the unit’s front display screen, from the
remote control unit, or from the footswitch. Selecting a new step results in a voice
confirmation. (The user has the ability to turn the voice feature off via the Custom /
Doctor Settings / Sounds dialog.)

3.3 Stationary Step Buttons

Stationary step buttons are always present in Surgery screens to support Coag and
Ant Vit. These two steps are selectable from the display screen and remote control,
but can be exited using either the display screen, remote control, or footswitch (if
footswitch button programmed for Step+, Step–, Step ±) when pedal is in position 0
or 1.

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SURGERY MODES

Phaco Mode of Operation

When a phaco (phacoemulsification) step is selected, IOP target, irrigation, aspiration,
longitudinal power (phaco power), and torsional amplitude (ultrasonic oscillations) are
provided by the handpiece. In this mode of operation longitudinal power and ultrasonic
oscillations alternately turn On and Off. Ultrasound power and torsional displacement of the
phaco tip is proportional to the longitudinal and torsional settings displayed on the console
front panel. The user has the ability to adjust the IOP target, aspiration rate, vacuum levels,
longitudinal power, and torsional amplitude
at any time during the surgical procedure via sional
or plitude
their respective adjustment dialogs or remote m

T
A
control. For best performance, use tips
wer
recommended by your Alcon representative. ud i n a l Po
git
Lon
Power/Amplitude
The Longitudinal Power and Torsional Amplitude settings are increased or decreased
via adjustment dialogs in increments of 5% from a minimum of 0% to a maximum of
100%. Power and amplitude to the handpiece is controlled by one of two methods: fixed
or linear footpedal control.

• If fixed footpedal control is selected (equal start and end values in footpedal
position 3), the end value indicates the fixed power or amplitude delivered to the
handpiece. To increase or decrease the value, press an oval display button to bring
up the adjustment dialog window (see left image in Figure 2-79 for example of
fixed Longitudinal Power adjustment) and use the adjustment buttons to increase
or decrease the fixed value.

• If linear footpedal control is selected (unequal start and end values through footpedal
position 3), the starting and end values in the dialog indicate increasing or decreasing
power or amplitude throughout footpedal position 3. To change the starting and end
values, press an oval display button to bring up the adjustment dialog window (see
right image in Figure 2-79 for example of Torsional Amplitude adjustment) and use
the adjustment buttons to increase or decrease the starting and end values.

Figure 2-79 Power/Amplitude Dialogs - These two screens show a fixed Longitudinal Power dialog
(left) and a linear Torsional Amplitude dialog (right), identified by the horizontal and diagonal lines in
their oval display buttons. See Figure 2-67 for description of Oval Display Button Dialog.

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 Phaco Timing Configurations
In footpedal position 3, longitudinal power and torsional amplitude are delivered
to the phaco tip through a variety of timing configurations. Depending on the mode
selected (Continuous, Pulse, Burst) the timing can be continuous, or can include off-
times between longitudinal/torsional pulses. The three modes are explained below.

• Continuous Phaco Mode - In this mode phaco power is delivered 100% of the
time in footpedal position 3. When the Longitudinal power or Torsional amplitude
setting is set to 0% (no power), then only torsional or longitudinal phaco power is
delivered, for 100% of the time, to the handpiece tip. This allows the user to have
continuous ultrasonic longitudinal power or torsional amplitude, if so desired. If
longitudinal power and torsional amplitude are both used, then continuous phaco
provides 20% of its duty cycle for longitudinal power and torsional ultrasonic
oscillations for the remaining 80% when in footpedal position 3, and repeats this
cycle over and over again as long as the footpedal is in position 3. This produces
continuous alternations between longitudinal power and torsional amplitude.

The user can select any fixed value or linear start and end values for both
Longitudinal Power % and Torsional Amplitude % when in footpedal position 3
by invoking their associated oval display button dialogs.

Figure 2-80 Continuous Phaco Surgery Screen - In this case Torsional amplitude is
delivered at 20% amplitude for 100% of the time.

RESTING (position 0)

IRRIGATION (position 1)

PEDAL
FOOT IRR + ASPIRATION (position 2)

IRR + ASP + PHACO (position 3)

FOOTSWITCH ASSEMBLY

Figure 2-81 Footpedal Control In Phaco Modes of Operation

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 • Pulse Phaco Mode - When operating in this mode of operation, longitudinal
power and torsional amplitude turn On and Off at a power and frequency
determined by the Pulse Rate (pps) setting, and on a duty cycle adjustable by
the operator (Time On %). The sum of Torsional Time On (%) and Longitudinal
Time On (%) cannot exceed 100%. If less than 100%, the remaining duty cycle,
or percent time Off, is an off-time.

For example, in the figures below, one pulse (torsional, longitudinal, off-time)
is 100 ms duration because of the selected pulse rate of 10 pps. Duration of
the phaco pulse, therefore, is 50 ms torsional (100 ms X 50%) plus 10 ms
longitudinal (100 ms X 10%) and the remaining 40 ms is an Off period.

If Torsional (%) Amplitude Limit or Longitudinal (%) Power Limit are set to zero,
then they contribute nothing to the pulse, and their duty cycles (Time On %) have
no effect.

50 ms (50% of 100 ms) at up to linear 40% torsional amplitude

10 ms (10% of 100 ms) at 35% fixed longitudinal power
Remaining 40 ms off period

100 ms
1 pulse
100 ms

1.0 second at 10 pps

Figure 2-82 Pulse Phaco Surgery Screen and Timing Diagram - In this case Torsional oscillations are
delivered at 40% amplitude for 50 ms, Longitudinal power is delivered at 35% power for
10 ms, and no power/oscillations are delivered for 40 ms.

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 • Burst Phaco Mode - When operating in this mode of operation, torsional burst is
followed immediately by longitudinal burst, followed by a pause. Duration of the
phaco burst is determined by the settings on the panel; for example, in the Figures
below the On Time is 70 ms torsional, 30 ms longitudinal, and the duration of the
Off Time is determined by the linear position of the footpedal in position 3. At
the beginning the Off Time is equal to 2500 ms, and it is gradually reduced as the
footpedal is depressed. When the footpedal is depressed all the way, the Off Time
will be equal to that set on the panel – 30 ms in the given example.

If Torsional (%) Amplitude and/or Longitudinal (%) Power are set to zero, then
there are no torsional or longitudinal contributions to the burst, and their duty
cycles (On Time ms) have no effect.

70 ms at up to linear 40% torsional amplitude

30 ms at 35% fixed longitudinal power
Variable off time determined by linear footpedal
position from 2500 ms to 30 ms at full depression

1 burst

1 burst

Time

Figure 2-83 Burst Phaco Surgery Screen and Timing Diagram - In this case Torsional oscillations are
delivered at 40% amplitude for 70 ms, Longitudinal power is delivered at 35% power for 30
ms, and the off time becomes reduced as the footpedal is depressed through position 3.

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 Irrigation/Aspiration Mode of Operation

Irrigation/Aspiration mode (Irr/Asp) provides irrigation and simultaneous peristaltic

aspiration for use with I/A handpieces and tips. Irrigation/Aspiration control supports
all surgical steps except coagulation.

In Irr/Asp mode there are only two footpedal positions. Irrigation is provided in
footpedal positions 1 and 2; Aspiration is provided in footpedal position 2.

All Irr/Asp steps contain IOP target, vacuum, and aspiration fluidics control
parameters. These parameters are displayed in the lower control panel portion of the
Surgery Screen. The Surgery Control Panel in the upper portion does not contain any
surgical parameters, but does contain an indication of the step type; i.e., Irr /Asp.

The left screen in Figure 2-84 is an example of an Irr/Asp surgery screen. If the
AutoSert® injector step is enabled (Custom/Procedure Builder/New Step/AutoSert®), the
setup controls for the INTREPID® AutoSert® IOL Injector are displayed in the upper
control panel, as shown in the right screen (D/C cartridge selected). This allows the
nurse to prepare the AutoSert® Injector while the surgeon is performing Irr/Asp steps.

Figure 2-84 The Irrigation/Aspiration Surgery Screen

RESTING (position 0)

IRRIGATION (position 1)
DAL
TPE
FOO
IRR + ASPIRATION (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-85 Footpedal Control in I/A Mode of Operation

2.82
FOR REFERENCE ONLY 8065751772
 Vacuum Control
The operator can adjust the vacuum limit using the front display panel or the remote
control. The adjustable vacuum limit range is 0 to 700+ mmHg (0 to 933+ hPa),
where 700+ mmHg (933+ hPa) is limited by atmospheric pressure.

• Fixed Vacuum Control - Fixed vacuum control provides a fixed vacuum limit
when aspirating in footpedal position 2.

• Linear Vacuum Control - Linear vacuum control provides linear control of

vacuum in footpedal position 2. The actual vacuum limit is proportional to the
footpedal position, and tracks with footswitch penetration within the footpedal
position.

Aspiration Control
The operator can adjust the aspiration limit using the front display panel or the remote
control. The adjustable aspiration limit range is 5 to 60 cc/min (5 to 60 mL/min).

• Fixed Aspiration Control - Fixed aspiration control provides a fixed aspiration

flow rate through footpedal position 2.

• Linear Aspiration Control - Linear aspiration control provides linear control of

aspiration flow rate in footpedal position 2. Aspiration flow rate is controlled
linearly based on settings and by footpedal penetration in position 2

Using Fill Step for Irrigation/Aspiration

The Fill step can be added at any location in the procedure using the Custom/
Procedure Builder menu. It is recommended to add the Fill step before the first I/A
step to facilitate removal of air from the I/A handpiece prior to use. Adding the Fill
step after the last I/A step helps clean the I/A tip and handpiece.

When transitioned into the Fill step, irrigation and reflux will be enabled
simultaneously for up to 10 seconds. If Irrigation Fill is enabled in the Custom/System
Settings/General menu, this step will be Irrigation Fill, and irrigation will be enabled
without reflux.

8065751772 2.83
FOR REFERENCE ONLY
 AutoSert® IOL Injector Mode of Operation

The AutoSert® injector step can be added at any location in the procedure using the
Custom/Procedure Builder menu. The AutoSert® step is typically positioned before
the last I/A step.

The INTREPID® AutoSert® IOL Injector, after preparation with a loaded, single-
use cartridge, gives the surgeon footpedal control of AcrySof® lens insertion in
footpedal position 2. Prior to installation of the loaded cartridge, the user must
select the cartridge type which is to be inserted (D/C or INTREPID® cartridge). The
INTREPID® cartridge selection may not be available in all markets. Contact your
Alcon representative for the latest qualified lens/cartridge.

When connected to the Centurion® system, the IOL injector is calibrated, and if
successful, it becomes ready for use.

Figure 2-86 AutoSert® IOL Injector Screen

RESTING (position 0)

RESTING (position 1)
AL
T PED
FOO PRELOAD / INITIAL RATE
PAUSE
FINAL RATE (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-87 Footpedal Control in AutoSert® Injector Mode of Operation

2.84
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 • The Cartridge Selection button is the green button located to the right of the Load
Plunger button. Prior to selecting a cartridge, the button is labeled "None." After
selection the button is labeled with the particular cartridge selected (see left image
in Figure 2-88). The user must select either a D or C cartridge or an INTREPID®
cartridge before the INTREPID® AutoSert® IOL Injector can be prepared. The
cartridge type can be selected, the plunger can be loaded, and the IOL can be
preloaded in an I/A step or in the AutoSert® injector step. In the AutoSert® injector
step, once the cartridge type has be selected, the user can make changes to the
Initial Rate/Pause/Final Rate settings.

• The Load Plunger button is used to install a plunger, should this be required.

• The Preload IOL button is used by the nurse to prepare the IOL injector by
advancing the lens to the preload lens position. Alternatively, the doctor
can simply press the footpedal into position 2 and the preload activity will
automatically proceed.

• The Retract button is used to retract the handpiece plunger when lens insertion is
completed or when otherwise necessary. Alternatively, pressing and holding the
Retract button (Reflux) on the footswitch can also be used to retract the inserter.

During each of these activities a blue Progress Bar appears to show the activity,
and a red Cancel button also appears that allows the user to stop the activity at that
point (see right image in Figure 2-88). Note: If the preload and retract activities are
controlled with the footswitch, the progress bar and Cancel button do not appear.

After lens insertion (Initial Rate, Pause, Final Rate), the footpedal must be released
and the Retract button pressed to retract the inserter.

The footpedal can be released out of position 2 during these steps, causing a pause in
the insertion activity. Pressing into position 2 again causes the activity to resume from
the point it stopped.

Progress Bar
Cancel Button

Figure 2-88 AutoSert® Injector Setup - Using the AutoSert® injector feature cannot be done until a
cartridge type is selected by pressing the None button (left image). After selecting the cartridge type,
the plunger can be loaded, the IOL can be preloaded (right image), the Initial Rate/Pause/Final Rate
settings can be adjusted, and then the lens can be inserted.

8065751772 2.85
FOR REFERENCE ONLY
 • Initial Rate (mm/s) - Once the lens is at the Preload Lens position, the Initial Rate
setting (mm/s) controls the fixed delivery velocity up to the Pause position.

• Pause (s) - Once the Pause position is reached, a preprogrammed pause in forward
advancement is initiated. This momentary pause allows internal stresses on the
lens to be relieved, thus ensuring proper lens delivery.

• Final Rate (mm/s) - This setting controls the fixed or linear velocity at which the
lens is injected into the eye.

PRECAUTION: The default values for the Initial Rate and Pause ensure proper IOL
injection over a worst case range of IOL size and ambient temperature conditions.
Please refer to the INTREPID® AutoSert® IOL Injector DFU and consult with your
Alcon representative for additional guidance in adjusting these parameters for your
environment.

CAUTIONS
• Do not ultrasonically clean the IOL injector connector. Ultrasonic cleaning of IOL
injector connector will cause irreparable damage.
• Use care when handling handpiece, particularly when cleaning. Always clean
handpiece over a surface cushioned with a pad or rubber mat.
• Be sure handpiece cable connector is dry before connecting it to the console.
• Do not disconnect cable connector from Centurion® system console until the
handpiece plunger is fully retracted.
• Do not immerse the IOL injector in any fluid when the plunger is not retracted.
• As part of a properly maintained surgical environment, it is recommended that
a backup IOL injector be made available in the event the AutoSert® IOL injector
handpiece does not perform as expected.

WARNINGS!
• The INTREPID® AutoSert® IOL Injector is non-sterile and must be cleaned and
sterilized prior to, and immediately after, each use.
• Never immerse the IOL injector in liquid after autoclaving; allow it to air cool for at
least 15 minutes. Quenching could result in a potentially hazardous condition for
the patient.
• The AutoSert® IOL Injector delivery system is for the implantation of Alcon qualified
AcrySof® foldable IOLs. Unqualified lenses shall not be used with the system. See
INTREPID® AutoSert® IOL Injector DFU or AcrySof® IOL DFU, or contact your Alcon
representative, for qualified lens/cartridge combinations.
• The cartridge/IOL combination listed in the DFU, along with Alcon settings, has
been validated per section 5 of BS EN ISO 11979-3:2006. Appropriate use of injector
handpiece settings is important for successful IOL implantation. Inappropriate use
of settings may lead to a potentially hazardous condition for the patient.
• Fully retract plunger before detaching nosecone from AutoSert® IOL Injector;
otherwise, this could expose non-sterile portion of shaft and result in a potentially
hazardous condition for the patient.
• For the intended IOL to be implanted, the proper Cartridge profile must be selected
from the driving console, and the proper plunger must be attached to the AutoSert®
IOL Injector. Failure to do so can result in a potentially hazardous condition for patient.
• The metal reusable plunger must be sterilized after each use. The reusable plunger
is to be installed onto the handpiece or into the wrench prior to sterilization.

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 Coagulation Mode of Operation

The Coagulation mode provides approximately 1.5 MHz frequency bipolar

coagulation to drive a brush or forceps in footpedal position 2. The percentage of
maximum available coagulation power can be set from 0% to 100% by pressing the
Power display button to bring up the adjustment dialog window. In the window select
either fixed or linear footpedal control, then press the up or down arrows to increase
or decrease the power limit (s).

Coagulation begins upon entering footpedal position 2, and an audible tone is

initialized. As in all other steps, coagulation settings are retained in memory so that
when re-entering the Coagulation step, the previous settings are displayed.

• Fixed Coagulation Control -Fixed control provides bipolar coagulation at the

preset limit when the footpedal enters position 2.

• Linear Coagulation Control - Coagulation Power begins at its lower setting

when entering footpedal position 2, and it reaches its maximum setting when the
footpedal is fully depressed.

Figure 2-89 The Coagulation Screen

RESTING (position 0)

RESTING (position 1)
DAL
TPE
FOO
COAGULATION (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-90 Footpedal Control in Coagulation Mode of Operation

8065751772 2.87
FOR REFERENCE ONLY
 WARNINGS!
• Do not use the coagulation function on patients with pacemakers or implanted
defibrillatory devices. If electrosurgery is used on patients with implanted
cardiac pacemakers or defibrillatory devices or pacemaker electrodes, be
aware that irreparable damage to the pacemaker or defibrillatory device and its
function may occur and lead to ventricular fibrillation. Please check with the
pacemaker or defibrillatory device manufacturers for their recommendations.

• Failure of the HF surgical equipment (coagulation circuitry) could result in

an unintended increase of output power.

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FOR REFERENCE ONLY 8065751772
 Anterior Vitrectomy Mode of Operation
The Anterior Vitrectomy (Ant Vit) mode is used to drive a 23 gauge, pneumatically
operated, Centurion® vitrectomy cutter. Fixed and linear control of the Cut Rate is
adjustable from 1 to 4000 cuts per minute in four of five vitrectomy modes (only
fixed control in peripheral iridotomy mode). Fixed and linear control of Vacuum and
Aspiration is provided in all five vitrectomy modes.

A switch on the footswitch may be assigned to enable and disable the Vit Cutter
using the Custom/Doctor Settings/Footswitch tab. When the Vit Cutter is disabled,
I/A functionality in footpedal position 2 is unchanged, but the Vit Cutter does not cut
and the message “Cut Disabled” is displayed. The assigned Vit Cutter switch may be
pressed in any footpedal position, and the function takes effect immediately.

If desired, an on-screen Vitrectomy Setup dialog appears when entering the I/A
step to help the user prepare the vitrectomy cutter for surgery (see Figure 90). This
feature can be enabled in the Custom/Doctor Settings/General tab, then pressing the
On button in the Vit Setup window. Now when entering the Ant Vit step a window
appears to guide the user through the vitrectomy setup.

Figure 2-91 Anterior Vitrectomy Setup Dialog - This dialog appears when entering the
Ant Vit step, but it must be enabled in the Custom/Doctor Settings/General tab.

RESTING (position 0)

IRRIGATION (position 1)

EDAL
FOOTP
IRR + ASPIRATION + CUTTING (position 2)

FOOTSWITCH ASSEMBLY

Figure 2-92 Footpedal Control In Anterior Vitrectomy Mode of Operation (except for I/A
Cut which is Resting/Irrigation/Irrigation+Aspiration/Irrigation+Aspiration+Cutting)

8065751772 2.89
FOR REFERENCE ONLY
 • Anterior Vitrectomy (Anterior Vit) - The Anterior Vitrectomy mode is the system's
default setting. This mode offers a high cut rate of up to 4000 cpm, vacuum up
to 700+ mmHg (933+ pHa), and an aspiration rate up to 60 cc/min (60 mL/min).
Each of these settings are footpedal controlled at a fixed rate or linearly.

Figure 2-93 Anterior Vitrectomy (Anterior Vit) Screen

• Epinucleus Removal (Epi Removal) - The Epinucleus Removal submode provides

settings that assist in epinucleus removal while vitreous is present during surgery.
As default settings, the linear cut rates (1500 down to 500 cpm) and linear
vacuum limit (0 up to 500 mmHg [0 up to 667 hPa]) in opposing slopes provide
vitreous removal at start of footpedal postion 2, and epinucleus removal at the end
of footpedal position 2.

Figure 2-94 Anterior Vitrectomy (Epi Removal) Screen

2.90
FOR REFERENCE ONLY 8065751772
 • Irrigation/Aspiration Cut (I/A Cut) - Irrigation is provided in footpedal position 1;
irrigation and aspiration in position 2; and irrigation, aspiration, and cutting in
position 3.

Figure 2-95 Anterior Vitrectomy (I/A Cut) Screen

• Peripheral Iridotomy (Peripheral Irid) - For a Peripheral Iridotomy using the

vitrectomy probe, the open port of the probe is placed on the iris while aspirating.
Once an occlusion of the iris has occurred and vacuum stability is reached, further
pressing to the very end of footpedal travel will engage the cutter at a fixed cut rate
as indicated by the Cut Rate setting.

Figure 2-96 Anterior Vitrectomy (Peripheral Irid) Screen

8065751772 2.91
FOR REFERENCE ONLY
 • Visco Aspiration (Visco Asp) - Visco Aspiration is a submode that uses the
vitrectomy probe for viscoelastic removal after an anterior vitrectomy. Using
default settings, the high cut rate (4000 cpm), high linear vacuum (0 to 650
mmHg [0 to 867 hPa]), and higher aspiration rate (50 cc/min [50 mL/min])
facilitate easy viscoelastic removal with a Vitrectomy probe.

Figure 2-97 Anterior Vitrectomy (Visco Asp) Screen

2.92
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION THREE
OPERATING INSTRUCTIONS

INTRODUCTION
This section details a recommended setup and check‑out procedure for the Centurion®
Vision System. The steps on the following pages cover preparation for cataract lens
removal surgery including capsulotomy, irrigation and aspiration, coagulation, and
vitrectomy using packs supplied by Alcon.

The Centurion® Vision System, including Alcon-approved consumables and accessories,

constitutes a complete surgical system and is intended exclusively for use by licensed
ophthalmic surgeons and their surgical teams. These surgical teams are experienced
at conducting phacoemulsification procedures in a properly-maintained surgical
environment (qualified personnel, availability of backup equipment) and are familiar with
the operation of the equipment used as outlined in operator’s manuals and directions for
use (setup/checkout procedures to be completed before the surgical procedure; processing
of reusable devices; maintenance; etc.).

The procedures are divided into two columns and presume a surgical team of four people:
Surgeon and Scrub Nurse in the sterile field, a Circulating Nurse in the non‑sterile field,
and a Sterilization Technician. In the left column a directive is given; in the right column
the responsible team member is identified.

Any problems pertaining to setup and check‑out procedures should first be directed to
the Troubleshooting section of this manual. If questions still exist, contact the Alcon
Technical Services Department or your local Alcon representative.

POWER UP SEQUENCE
System power-up is initiated when when the Power switch is turned on and the Standby
switch is pressed. After some delay (during which the Alcon splash screen is displayed) a
full-screen animation concluding with "Centurion® Vision System" is displayed. During
power-up the following are displayed at the bottom of the Startup Screen:
Release: REL_xx.xx Copyright 2013 Novartis AG
Access U.S. Patents list on About Dialog 2013/xx/xx 10:20

After power-up, the Setup Screen is entered. If there are no user-defined doctors, then Alcon
Settings becomes the currently-selected doctor, otherwise the Select Doctor dialog is opened.

SHUT DOWN SEQUENCE

System shutdown may be initiated by pressing the Custom/Shutdown System button, or
by pressing the Standby switch for at least two seconds, then a Shut down the system?
confirmation dialog is displayed. If no FMS, phaco handpiece, or IOL handpiece is
connected to the system and the Standby switch is pressed, the shutdown proceeds
immediately. In some system Fault conditions it may be necessary to press the Standby
switch for at least five seconds before shutdown is initiated.

8065751772 3.1
FOR REFERENCE ONLY
INITIAL SYSTEM SETUP

1. Remove footswitch from cradle on rear of system and set on floor. If using Circulating Nurse
cabled footswitch, plug cable into one-of-two connectors at bottom of
console's front panel. Ensure treadle and switches are not depressed.

2. Fold instrument tray down into the horizontal position. If remote control is Circulating Nurse
to be used during surgery, pull a left or right loop out from the instrument
tray and place the remote control in it.

3. Plug main power cord into a suitable wall outlet or receptacle. Turn Power Circulating Nurse
switch ON (located at the bottom of the rear panel; this switch remains ON
in the I position). Turn system power ON using the Standby switch located
at the top of the right side panel.

WARNINGS!
• To avoid risk of electric shock, this equipment must only be connected
to a supply mains with protective earth (ground).
• Do not use multiple portable socket outlets with this system.

4. After power-up, the Setup Screen is entered. If there are no user-defined Circulating Nurse
doctors, then Alcon Settings becomes the currently-selected doctor. If
there are user-defined doctors, the Select Doctor dialog appears allowing
the user to select an available doctor.

If creation of a new doctor is desired, press the Doctor Name button, press
the Manage Doctors button, and follow the on-screen prompts.

WARNING!
Ensure that appropriate Centurion® system parameters and system
settings are selected prior to starting the procedure. Parameter and
system settings include, but are not limited to, ultrasound mode,
ultrasound power, vacuum, aspiration flow rate, bottle height, IOP, etc.

5. Verify remote control is functional by pressing its buttons and observing Circulating Nurse
the system's actions.

6. Inspect the O‑rings on the Ultraflow™* II I/A handpiece tip. If damaged, Sterilization
the O‑rings must be replaced using the Ultraflow™* O‑ring tool prior to Technician
sterilization.

7. Clean, inspect, and sterilize the instruments according to hospital procedure. Sterilization
Technician
CAUTION
The phaco handpiece must be at room temperature before use. Allow
handpiece to air cool after steam autoclave (at least 15 minutes). Never
immerse in liquid to cool.

3.2
FOR REFERENCE ONLY 8065751772
CENTURION® FMS PACK SETUP PROCEDURE

1. Open FMS pack and aseptically transfer contents to sterile field. Circulating Nurse

2. Extend front or rear wire loop from the instrument tray. Drape tray support Circulating Nurse
cover over the tray, remote control, and support arm, then push cover down and Scrub Nurse
into the loop to form a pouch for the handpiece.

3. For Active Fluidics™ technology, rotate upper work surface to the side, open Circulating Nurse
Active Fluidics™ compartment door, gently lower bag of BSS® irrigating
fluid into the bag bay, and slide the compartment door shut.

For gravity fluidics, hang a container of BSS® irrigating fluid from IV pole. Circulating Nurse

WARNING!
Use of BSS® irrigating fluid bags other than those approved by Alcon
for use with Active Fluidics™ technology can result in patient injury or
system damage.

4. Grasp Fluidic Management System (FMS) and remove paper band from Scrub Nurse
tubing. Uncoil tubing and place in pouch.

5. Hold FMS by handle, angle it toward the lip on bottom of fluidic module, Scrub Nurse
and press top forward to insert into housing, all in one motion. Ensure that
the drain bag hangs freely, and that tubing does not fall out of pouch.

Prime, Vacuum, and Vent Test

The setup screen is automatically entered at startup or upon removal of the
FMS after completion of a procedure. If not in setup screen, press the Setup
button, or access the setup screen via the remote control.

6. For Active Fluidics™ technology, spike BSS® irrigating fluid administration Circulating Nurse
line from FMS into the bag of BSS® irrigating fluid secured within the Active or Scrub Nurse
Fluidics™ bag bay. Verify compartment door is fully closed.

For gravity fluidics, spike BSS® irrigating fluid administration line from Circulating Nurse
FMS into the container of BSS® irrigating fluid hanging from IV pole, then
squeeze drip chamber to fill approximately 2/3 to 3/4 full.

7. Connect FMS tubing together to create a fluidics loop: Connect FMS tubing Scrub Nurse
with female aspiration luer to FMS tubing with male irrigation luer.

8065751772 3.3
FOR REFERENCE ONLY
8. Ensure correct Doctor and Procedure setting are selected. Press Prime FMS Scrub Nurse
on the Setup screen or Enter on the remote control to initiate the priming/
test sequence. The system performs three functions: draw fluid, vacuum test,
and vent test.

For gravity fluidics the IV pole automatically elevates to the priming position
during the priming test, then returns to its home position after successful
completion the testing sequence.

WARNINGS!
• IV pole rises automatically. To avoid stretching drip chamber tubing,
and possibly pulling drip chamber out of bottle, tubing must hang
freely with no interference.
• If using gravity fluidics, keep clear of IV pole when it is in motion to
prevent skin, hair, and/or clothing from becoming trapped in the IV pole
mechanism.

After successful completion of the priming sequence, the FMS prime status
indicator at top of display screen (Active Fluidics™ FMS or Gravity FMS)
changes from red (not primed) to green (primed), and the setup automatically
switches to the Fill step.

If the priming/test sequence fails, an advisory message is displayed.

3.4
FOR REFERENCE ONLY 8065751772
 Phaco Handpiece Setup and Test

9. Thread U/S tip onto phaco handpiece (see Figure 3-1). Tighten firmly using Scrub Nurse
the tip wrench. Remove wrench and retain for tip removal. If tip is not
securely attached, an Event message may be generated and/or inadequate
tuning will occur.

CAUTION
Do not use the disposable tip wrench for subsequent cases; stripping of
the tip wrench may occur.

10. Match proper color coding of infusion sleeve with selected tip (see Table Scrub Nurse
3-1). Tip of sleeve should clear bevel on U/S tip by 1-2 mm (see Figure 3-2),
and orient port holes as shown. Avoid twisting the sleeve.

THREADED END OF U/S TIP

TIP WRENCH CENTURION® OZil® Handpiece

Figure 3-1 U/S Tip/Wrench Assembly

Infusion Sleeve Recommended

Handpiece Tips Sleeve Color
Size and Type Incision Size

0.9 mm MicroTip and 0.9 mm ABS® MicroTip

0.9 mm Tapered ABS® MicroTip 0.9 mm High Infusion Sleeve Light Purple 3.2 mm
0.9 mm Flared ABS® MicroTip
0.9 mm Mini-Flared ABS® Tip
0.9 mm ABS® Mini Tip
0.9 mm ABS® INTREPID® Balanced Tip
0.9 mm Micro Sleeve Dark Purple 2.75 mm
0.9 mm ALCON® UltraChopper® Tip
Standard I/A, Silicone I/A, INTREPID® I/A Tip

0.9 mm Flared ABS® MicroTip

0.9 mm Mini-Flared ABS® Tip 0.9 mm Ultra Sleeve Red 2.2 mm
0.9 mm ABS® Mini Tip
0.9 mm ABS® INTREPID® Balanced Tip
0.9 mm ALCON® UltraChopper® Tip 0.9 mm Nano Sleeve Orange 1.8 mm
Silicone I/A, INTREPID® I/A Tip

0.7 mm Ultra Sleeve Yellow 2.2 mm

0.7 mm ABS® Mini Tip
0.7 mm ABS® INTREPID® Balanced Tip
0.7 mm Nano Sleeve Gray 1.8 mm

Table 3-1 Table of Phaco Handpiece Tips and Corresponding Infusion Sleeves.

8065751772 3.5
FOR REFERENCE ONLY
 Infusion Sleeve

CENTURION® OZil® Handpiece

U/S Tip

1.0 to 2.0 mm

U/S Tip
Port Hole turned 90° to tip bevel
Infusion Sleeve

Straight Kelman® Flared Flared

Straight Kelman®

Figure 3-2 Phaco Handpiece Tip/Infusion Sleeve Preparation

Irrigation Line
(clear male luer with white luer lock)

Aspiration Line
(blue female luer)
N
URIO
CENT

Connect cable to front panel connector

identified by handpiece icon:
• CENTURION® OZil® handpiece
• INFINITI® OZil® handpiece

Figure 3-3 Connect Phaco Handpiece to FMS Tubing and Centurion® System Connector Panel
(CENTURION® OZil® handpiece shown).

Place handpiece
vertically in pouch
formed with drape

Slide test chamber

over handpiece tip

BSS® irrigating fluid

in test chamber

Figure 3-4 Preparing Test Chamber and Placing Handpiece in Pouch.

3.6
FOR REFERENCE ONLY 8065751772
11. Remove protective cap from handpiece cable connector by retracting its Scrub Nurse
sheath and releasing cap. Line up red dot on handpiece cable connector with
red dot on front panel connector and plug cable into console (see Figures
2-2 & 3-3). If CENTURION® OZil® handpiece, plug into one of the top two
connectors. If INFINITI® OZil® handpiece, plug into bottom connector.

12. From FMS, connect the female luer on aspiration line to male aspiration port Scrub Nurse
on handpiece. Connect male luer on irrigation line to female irrigation port
on handpiece. If Centurion® handpiece, turn the white luer lock clockwise
to lock irrigation fitting to handpiece (see Figure 3-3).

13. Hold handpiece with tip pointed down into test chamber (see Figure 3-4) Scrub Nurse
and activate Fill on the setup screen. While observing stream of fluid from
irrigation and aspiration ports, fill test chamber completely and slide it over
end of handpiece. Ensure no air bubbles are present in test chamber. Press
handpiece into instrument tray pouch with tip pointed up, and secure irrigation/
aspiration lines to clips on top of tray. Ensure tubing is not kinked.

WARNINGS!
If stream of fluid is weak or absent while filling test chamber, good fluidics
response will be jeopardized. Good clinical practice dictates the testing
for adequate irrigation and aspiration flow prior to entering the eye.

Ensure that the tubings are not occluded during any phase of operation.

When using a bimanual procedure, ensure the irrigation handpiece and

settings have sufficient flow characteristics. Use of irrigation handpieces
or settings with insufficient flow characteristics may result in a fluidic
imbalance and may cause a shallowing or collapsing of the anterior chamber.

If an INFINITI® OZil® handpiece is connected to the bottom connector, and

Ultrachop step is added to surgery steps, press the Swap Phaco / UltraChop
button and repeat steps 12 and 13.

14. Activate Test Handpiece on the setup screen. The test consists of a handpiece Scrub Nurse
tuning exercise and fluidic flow check. If handpiece fails tuning or flow test,
an advisory is displayed. The handpiece tuning process can be aborted at any
time by pressing cancel (X).

WARNINGS!
If the handpiece test chamber is collapsed after tuning, there is a potential
of low irrigation flow through the handpiece and may result in a fluidic
imbalance. This, in turn, may cause a shallowing or collapsing of the
anterior chamber.

Good clinical practice dictates testing for adequate irrigation, aspiration

flow, reflux, and operation as applicable for each handpiece prior to
entering eye.

8065751772 3.7
FOR REFERENCE ONLY
15. After successfully testing handpiece you must adjust and verify the Patient Scrub Nurse
Eye Level (PEL) until the console PEL light aligns with the patient's eye
level (see Figure 3-5). If enabled, a PEL verification step is provided in the
setup screen. When alignment is complete, press the green check mark to
enter the Surgery Screen for the first step of the procedure.

PRECAUTION: After a successful tuning of the handpiece, and if PEL

verification is disabled, the first step of the lens removal procedure is entered
without verifying PEL.

CENTURION
lue
Va
VISION SYSTEM

E L
P
ight
o t t l e He idics
B lu
ity F
for Grav

)
EL
(P
v el
e Le
t Ey
tien
Pa

Figure 3-5 Setting Patient Eye Level (PEL).

3.8
FOR REFERENCE ONLY 8065751772
IRRIGATION/ASPIRATION HANDPIECE SETUP

1. If using Ultraflow™* II I/A handpiece with threaded tip adapter, follow Scrub Nurse
the directions in this step. or
Sterilization
Thread I/A tip onto I/A handpiece. Tighten firmly using the I/A tip wrench. Technician
Remove I/A tip wrench and retain for future tip removal.

CAUTION
Use of a tool other than Alcon tip wrench may cause damage to the
I/A tip and handpiece.

2. Thread infusion sleeve over the I/A tip until sleeve clears end of I/A tip Scrub Nurse
by 1-2 mm (see Figure 3-6). Avoid twisting of the Sleeve. Orient port
holes as shown and ensure that aspiration holes are not obstructed.

Infusion Sleeve I/A Tip UltraFlow™* II I/A Handpiece

Aspiration Holes in I/A Tip

1.0 to 2.0 mm Infusion Sleeve

Figure 3-6 I/A Handpiece Tip/Infusion Sleeve Preparation.

3. Remove aspiration and irrigation lines from the phaco handpiece Scrub Nurse
and connect to the I/A handpiece. For I/A handpieces equipped with
a locking irrigation luer, turn the white luer lock clockwise to lock
irrigation line to handpiece.

4. In Surgery screen, and with handpiece level with instrument tray, Surgeon
depress footswitch to position 1 to stream irrigation fluid from the or
irrigation port. Activate the reflux function to stream fluid from the I/A Scrub Nurse
tip’s aspiration port. Observe the stream of irrigating fluid from the
irrigation and aspiration ports. Ensure no air bubbles remain in irrigation
or aspiration pathways before continuing procedure.

WARNING!
If stream of fluid is weak or absent, good fluidics response will be
jeopardized. Good clinical practice dictates the testing for adequate
irrigation and aspiration flow prior to entering the eye.

8065751772 3.9
FOR REFERENCE ONLY
INTREPID® AUTOSERT® IOL INJECTOR SETUP

1. If AutoSert® injector step is not already shown at bottom of Surgery Circulating Nurse
screen for this doctor, add it to the steps using the Custom/Procedure or
Builder/New Step window. The AutoSert® injector step is typically Scrub Nurse
positioned before the last Irr/Asp step.

2. Plug INTREPID® AutoSert® IOL Injector Handpiece cable into one of Scrub Nurse
the top two handpiece connectors on the front connector panel. (Usually
it is the second of the two as the first is used by the phaco handpiece.)

3. Enter the AutoSert® injector step (or Irr/Asp step with AutoSert® setup in Scrub Nurse
its Surgery Controls area).

Select a Cartridge
Prior to loading plunger and preloading IOL, the user must select the
cartridge type which is to be inserted (D/C or INTREPID® cartridge).
With no cartridge selected, the cartridge type button is labeled "None."

4. Press the green cartridge type button to make a selection (INTREPID® Scrub Nurse
cartridge selection may not be available in all markets). Contact your
Alcon representative for the latest qualified lens/cartridge.

Remove a Plunger
It may be necessary to remove one type of plunger and replace it with
another type in the sterile field to accommodate either the D/C cartridge
or INTREPID® cartridge.

5. With plunger fully retracted, remove cartridge from IOL injector

handpiece.

6. Detach nosecone from IOL injector handpiece by rotating the nosecone Scrub Nurse
counter-clock-wise, then carefully sliding it away from the IOL injector
handpiece so it does not deflect the plunger.

7. With nosecone removed (see Figure 3-7), remove the plunger by Scrub Nurse
grasping it where indicated and pulling it away from IOL injector
handpiece.

8. Re-attach nosecone onto IOL injector handpiece. Scrub Nurse

Grasp plunger here

and pull away from IOL handpiece

Figure 3-7 Removing Plunger from INTREPID® AutoSert® IOL Injector.

3.10
FOR REFERENCE ONLY 8065751772
Load a Plunger
If a plunger needs to be installed, perform this procedure when an I/A
step or AutoSert® injector step is entered. The IOL injector handpiece
can be prepared with two types of plungers: the reusable metal plunger
or the single-use soft tip plunger. The reusable metal plunger is designed
for use with Monarch C and D cartridges. The single-use soft tip plunger
is designed for use with the INTREPID® cartridge.

9. Slide sterile plunger into sterile wrench, then connect plunger/wrench Scrub Nurse
onto nosecone of sterile IOL injector handpiece. Press Load Plunger
button (See Alcon® INTREPID® AutoSert® IOL Injector Handpiece DFU).

10. After plunger is loaded onto nosecone of sterile IOL injector handpiece, Scrub Nurse
remove wrench. The IOL injector handpiece is ready for the IOL cartridge.

Preload an IOL
Prior to entering the eye, the plunger must be moved forward to the
preload lens position.

11. Load IOL into cartridge, then insert loaded IOL cartridge onto tip of Scrub Nurse
IOL injector handpiece (See Alcon® INTREPID® AutoSert® IOL Injector
Handpiece DFU).

12. Press Preload IOL button. The AutoSert® handpiece is ready for use Scrub Nurse
when the preload sequence is complete.

Make Final Adjustments

13. In the AutoSert® injector step, and prior to inserting the lens into the Circulating Nurse
patient's eye, set the doctor's preferred Initial Rate (mm/s), Pause (s), and or
Final Rate (mm/s) settings. The Final Rate can be set for fixed or linear Scrub Nurse
delivery.

PRECAUTION: The default values for the Initial Rate and Pause ensure
proper IOL injection over a worst case range of IOL size and ambient
temperature conditions. Please refer to the INTREPID® AutoSert® IOL
Injector DFU and consult with your Alcon representative for additional
guidance in adjusting these parameters.

Cautions and Warnings for AutoSert® IOL injector on next page

8065751772 3.11
FOR REFERENCE ONLY
 CAUTIONS
• Do not ultrasonically clean the AutoSert® IOL Injector connector. Ultrasonic
cleaning will cause irreparable damage.
• Use care when handling AutoSert® IOL Injector, particularly when cleaning. Always
clean handpiece over a surface cushioned with a pad or rubber mat.
• Be sure handpiece cable connector is dry before connecting it to the console.
• Do not disconnect cable connector from Centurion® system console until the IOL
Injector plunger is fully retracted.
• Do not immerse the AutoSert® IOL Injector in any fluid when the plunger is not
retracted.
• As part of a properly maintained surgical environment, it is recommended that
a backup IOL injector be made available in the event the AutoSert® IOL injector
handpiece does not perform as expected.

WARNINGS!
• The INTREPID® AutoSert® IOL Injector is non-sterile and must be cleaned and
sterilized prior to, and immediately after, each use.
• Never immerse the IOL injector in liquid after autoclaving; allow it to air cool for at
least 15 minutes. Quenching could result in a potentially hazardous condition for
the patient.
• The AutoSert® IOL Injector delivery system is for the implantation of Alcon qualified
AcrySof® foldable IOLs. Unqualified lenses shall not be used with the system. See
INTREPID® AutoSert® IOL Injector DFU or AcrySof® IOL DFU, or contact your Alcon
representative, for qualified lens/cartridge combinations.
• The cartridge/IOL combination listed in the DFU, along with Alcon settings, has
been validated per section 5 of BS EN ISO 11979-3:2006. Appropriate use of injector
handpiece settings is important for successful IOL implantation. Inappropriate use
of settings may lead to a potentially hazardous condition for the patient.
• Fully retract plunger before detaching nosecone from AutoSert® IOL Injector;
otherwise, this could expose non-sterile portion of shaft and result in a potentially
hazardous condition for the patient.
• For the intended IOL to be implanted, the proper Cartridge profile must be selected
from the driving console, and the proper plunger must be attached to the AutoSert®
IOL Injector. Failure to do so can result in a potentially hazardous condition for patient.
• The metal reusable plunger must be sterilized after each use. The reusable plunger
is to be installed onto the handpiece or into the wrench prior to sterilization.

3.12
FOR REFERENCE ONLY 8065751772
CENTURION® ULTRAVIT® PROBE SETUP
(using Vitrectomy Setup dialog)

When the Anterior Vitrectomy step is entered, the Vitrectomy Setup dialog appears
(see Figure 3-8) unless turned Off in the Doctor Settings screen. This setup screen
assists the user through the proper set up and test of the selected probe.

If the Vitrectomy Setup dialog is turned Off, you can either turn the Vitrectomy
Setup dialog On (Custom/Doctor Settings/General), or proceed three more
pages to CENTURION® ULTRAVIT® PROBE SETUP (without using
Vitrectomy Setup dialog).

1. Peel lid and aseptically transfer contents of pack to sterile field. Circulating Nurse

2. Press the Ant Vit step button; the Vitrectomy Setup dialog appears. Scrub Nurse

NOTE: In the next few steps the user will be instructed to press buttons
on the Vitrectomy Setup dialog. These buttons can be pressed on the
display screen, or they can be activated using the Parameter Selection
keys and Enter key on the remote control.

3. Connect to console Vit port - Connect black and gray pneumatic tubing Scrub Nurse
connectors from the Centurion® UltraVit® Probe to left and right Vit
ports, respectively, on the front panel of the Centurion® Vision System
(see Figures 2-2 & 3-8 & 3-9). Turn tubing connectors clockwise until
they click securely in place.

Figure 3-8 Vitrectomy Setup Dialog - After performing a Vitrectomy Setup

step, pressing the Next button brings up the dialog for the next setup step.
In step 6, the Fill button allows the user to prime the probe and to fill a test
vessel for proper testing of the probe. Pressing the Test button initiates an
automated test sequence which verifies secure pneumatic connections, then
applies pneumatic activation at a reduced cut rate for visual verification of
probe actuation.

8065751772 3.13
FOR REFERENCE ONLY
 Irrigating Cannula Male Luer

Irrigation Tubing
From Centurion®
Fluidic Management
Centurion® UltraVit® Probe System (FMS)
Male Luer Female Luer
Aspiration Tubing

Gray Fitting
Clear
Pneumatic Tubing Connect to Centurion®
Front Connector Panel
Black Fitting
Black Striped

Figure 3-9 Preparation of Centurion® UltraVit® Probe and Irrigating

Cannula with Irrigation/aspiration and pneumatic tubings.

4. Connect aspiration tubing - Disconnect FMS irrigation and aspiration Scrub Nurse
tubing connectors from phaco handpiece. Connect FMS blue aspiration
tubing connector to probe's blue aspiration tubing connector (see Figure
3-9). Press Next button.

5. Connect irrigating cannula - Connect FMS white irrigation tubing Scrub Nurse
connector to irrigating cannula (see Figure 3-9). Press Next button.

6. Press Fill then press Test - Priming of the vitrectomy probe is required Scrub Nurse
prior to use. With tip of probe and irrigating cannula in a cup of sterile
fluid, press the Fill button. Ensure all air bubbles have been removed
from all tubing connected to the probe prior to use.

Verify probe actuation - While observing cutting port of probe, held Scrub Nurse
under surface of sterile fluid, press the Test button. The system intitiates
an automated test sequence confirming secure connections and facilitates
visualization of probe cutter by applying a brief period of reduced cut
rate. The cutter should fully open and close when actuated.

7. The Anterior Vit surgery screen appears on the front display panel. Scrub Nurse
Switching between five different vitrectomy types is done by pressing
the Mode button (Anterior Vit) at top center of surgery screen. The
vitrectomy probe is ready for surgery.

Cautions and Warnings for Centurion® UltraVit® Probe are on next page

3.14
FOR REFERENCE ONLY 8065751772
 CAUTION
Vitrectomy cutting performance may vary at high altitudes. Consult
Alcon Technical Service for additional information.

CENTURION® ULTRAVIT® PROBE WARNINGS!

The vitrectomy probe, a guillotine vitreous cutter, is intended for single use only.

Do not test or operate vitrectomy probe unless tip of probe is immersed in BSS ®
sterile irrigating solution or distilled water or is in surgical use. Irreparable
damage to the probe and tip can result if run dry.

Connect pneumatic tubing connectors from vitrectomy probe to console prior to

initiating prime of probe. Initiating prime of the vitrectomy probe, or running the
vitrectomy system, with one or both pneumatic connectors disconnected may
cause the flow of non-sterile air over the sterile field for a brief moment.

After filling and testing, and before surgical use, verify that the probe is
properly actuating and aspirating. This may require lowering cut rate to achieve
good visualization. The port should always remain in open position in footpedal
position 1. If cutting port is partially closed while in position 1, replace the probe.
Prior to entry into the eye, and with tip of probe in sterile irrigating solution,
the surgeon should step on the footpedal for visual verification that the probe
is cutting:
• If the cutter is observed to not fully close, or does not move when the probe
is actuated, replace the probe.
• If cutting port is partially closed while idle, replace the probe.
• If air bubbles are observed in the aspiration line or exiting the probe tip
during priming, replace the probe.
• If a reduction of cutting capability or vacuum is observed during the surgical
procedure, stop immediately and replace the probe.

8065751772 3.15
FOR REFERENCE ONLY
CENTURION® ULTRAVIT® PROBE SETUP
(without using Vitrectomy Setup dialog)

1. Peel lid and aseptically transfer contents to sterile field. Circulating Nurse

2. Press the Ant Vit step button; the Anterior Vit surgery screen appears. If Scrub Nurse
it is desired to have a Vit step as a part of the procedure, then it must be
added in the Procedure Builder.

3. Connect black and gray pneumatic tubing connectors from the Scrub Nurse
CENTURION® UltraVit® Probe to left and right Vit ports, respectively, on
the front panel of the Centurion® Vision System (see Figures 2-2 & 3-10).
Turn tubing connectors clockwise until they click securely in place.

4. Disconnect FMS irrigation and aspiration tubing connectors from phaco Scrub Nurse
handpiece. Connect FMS female luer aspiration connector to aspiration
line of vitrectomy probe. Connect FMS male luer irrigation connector to
irrigating cannula (see Figure 3-10).
Irrigating Cannula Male Luer

Irrigation Tubing
From Centurion®
Fluidic Management
Centurion® UltraVit® Probe System (FMS)
Male Luer Female Luer
Aspiration Tubing

Gray Fitting
Clear
Pneumatic Tubing Connect to Centurion®
Front Connector Panel
Black Fitting
Black Striped

Figure 3-10 Preparation of Centurion® UltraVit® Probe and Irrigating

Cannula with Irrigation/aspiration and pneumatic tubings.

5. Priming of the vitrectomy probe is required prior to use, and can be Scrub Nurse
performed using one of two methods. With tip of probe and irrigating
cannula in a cup of sterile fluid:
• Independently use irrigation by depressing the footpedal to position
1 to remove air bubbles from the probe’s irrigation line, and then use
reflux to remove air bubbles from the probe’s aspiration tubing.
• Use the Fill command, if enabled in the Procedure Builder and placed
before the Vit step, to simultaneously remove air bubbles from the
irrigation and aspiration lines. When completed, the system will
proceed to the selected Vit step.
Ensure all air bubbles have been removed from all tubing connected to
the probe prior to use.

6. Testing of the vitrectomy probe should be performed prior to use. With Scrub Nurse
tip of probe and irrigating cannula in a cup of sterile fluid, depress
footpedal to the cut position and observe probe's cutting port (to facilitate
visualization, reduce cut rate). The cutter should fully open and close
when actuated, and remain open when footpedal is released to position 0.

Cautions and Warnings for Centurion® UltraVit® Probe are on prior page
3.16
FOR REFERENCE ONLY 8065751772
COAGULATION HANDPIECE SETUP

1. Using aseptic techniques, plug new or sterilized handpiece cable Scrub Nurse
connectors into Centurion® Vision System front connector panel.

2. Plug connector into new or sterilized coagulation handpiece. Scrub Nurse

3. Coagulation handpiece is ready.

INTREPID® CAPSULOTOMY DEVICE SETUP

1. If the Capsulotomy step is not already shown at bottom of Surgery Circulating Nurse
screen for this doctor, it can be added using the Custom/Procedure or
Builder/New Step window. Scrub Nurse

2. Carefully remove INTREPID® Capsulotomy Device from plastic tray by Scrub Nurse
gently bending tray and exposing the top half of device.

CAUTION
Care should be taken as to not damage the distal end of the device.

3. Unwind cable and plug INTREPID® Capsulotomy Device into its Scrub Nurse
designated connector on the front connector panel.

4. Press the Test ICD button at bottom of Setup Screen. Scrub Nurse

5. Device must be enabled by pressing the Enable button at bottom of Scrub Nurse
Setup Screen, or by pressing the Reflux footswitch button. or
Surgeon

8065751772 3.17
FOR REFERENCE ONLY
 THIS PAGE INTENTIONALLY BLANK

3.18
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION FOUR
CARE AND MAINTENANCE

INTRODUCTION

This section of the manual is designed to inform the operator of basic care and
maintenance of the instrument. If a problem occurs on the instrument, contact
Alcon Technical Support or your local Alcon representative and give details of the
breakdown circumstances and effects. If there is an Event message, write down
the number and message exactly as it appears on the screen. From these elements,
a specialized technician will evaluate the problem and determine the maintenance
requirements.

For optimum performance, it is the user’s responsibility to schedule preventive

maintenance service on the system and its accessories at least one time each year.
Alcon’s Field Service Engineers are trained and equipped to provide the highest
quality of workmanship.
CAUTION
There are no operator replaceable parts other than the fuse. Contact Alcon
Technical Services for all servicing issues.

WARNING!
The Centurion® Vision System battery can only be serviced by a factory-trained
Alcon service engineer. Access by untrained personnel can lead to injury.

8065751772 4.1
FOR REFERENCE ONLY
UPON COMPLETION OF THE DAY'S SURGERY SCHEDULE

STEP ONE: Clean handpieces, cables, forceps, etc., as instructed in DFU's supplied
with each accessory.

WARNING!
If in the medical opinion of the physician a patient with a prion related disease
undergoes a high risk procedure, the instrument should be destroyed or be
processed according to local requirements.

STEP TWO: Remove bag of BSS® irrigating fluid from Active Fluidics™ bag bay, or
remove irrigation container from IV pole hanger, and set aside. Remove spike from
BSS® irrigating fluid and discard tubing.

STEP THREE: Eject FMS and discard.

STEP FOUR: Slide door shut over Active Fluidics™ bag bay, or flip IV pole hanger
to its storage position.

STEP FIVE: Select Custom/Shutdown from the Surgery Screen. Select OK. If used,
IV pole will go down to storage position before unit shuts off.

or

Press Standby power switch located at top of right side panel to remove operating
power from the system. If used, IV pole will go down to storage position before unit
shuts off.

WARNING!
If used, keep clear of the IV pole when it is in motion to prevent skin, hair, and/or
clothing from being trapped in the IV pole mechanism.

STEP SIX: Turn the primary AC power switch OFF. It is located at the bottom of the
rear panel.

STEP SEVEN: Disconnect the power cable from the wall receptacle and wind the
cable around the cord wrap.

4.2
FOR REFERENCE ONLY 8065751772
 STEP EIGHT: Inspect, and if required, clean footswitch bottom cover and under
footpedal with water, alcohol, or mild soap and water. Remove any debris (see Figure
4-1).
CAUTION
Debris, including fluid residue, stuck on footswitch bottom or under rear section
of treadle may cause temporary malfunction of the footswitch.

Clean and remove debris from

this area under the footpedal, and
from bottom of footswitch.

Figure 4-1 Footswitch Cleaning - Clean under footpedal and footswitch to remove
debris that can interfere with its operation.

STEP NINE: If required, the console panels, the footswitch, and the remote control
may be wiped with alcohol, mild soap and water, or any germicidal solution that is
compatible with the plastic parts.

CAUTIONS
• Do not clean console or accessories using solvents, abrasives, or any cleaner
that is not compatible with plastic parts made of LEXAN EXL9112. Damage
may result.
• Avoid spilling BSS® solution, or moisture of any kind, around the electrical
handpiece connectors.
• Do not spray any liquid (i.e. cleaning solution or water) upward into the
console vents.

STEP TEN: Hang the footswitch on the footswitch hanger/charging station at the
bottom of the rear panel.

8065751772 4.3
FOR REFERENCE ONLY
CARE AND CLEANING

The following tips are recommended for proper care of the Centurion® Vision System:
• The console panels, the footswitch, and the remote control may be wiped with
alcohol, mild soap and water, or any germicidal solution that is compatible with
the plastic parts; instructions begin on the prior page.
• The touch screen may be cleaned with a soft, non-abrasive cloth towel and a mild
commercially-available window cleaner. Apply the cleaner to the towel rather
than the touch screen.
• Follow cleaning and maintenance schedules outlined in this section of the manual.
• Periodically check chassis appearance.
• Pay attention to correct operation of controls, connectors, and indicators.
• Damaged hardware must be replaced to ensure safe operation. Call Alcon
Technical Services for assistance.

WARNING!
A qualified technician must perform a visual inspection of the following components
every twelve months:
• Warning Labels (see section one of this manual)
• Power Cord
• Fuses
In case of a deficiency, do not use the system; call Alcon Technical Services.

A qualified technician must check ground continuity and leakage current every
twelve months to ensure they are within the limits of the applicable standards (for
example: EN60601-1/IEC60601-1). Values must be recorded, and if they are above
the limits of the applicable standards, or 50% above initial measurement, do not use
the system; call Alcon Technical Services.

4.4
FOR REFERENCE ONLY 8065751772
STERILIZATION INSTRUCTIONS

The sterilization settings provided in Table 4-1 have been validated by Alcon Laboratories, Inc.
as being CAPABLE of sterilizing the instruments for re-use. It remains the responsibility of the
processor to ensure that the processing as actually performed using equipment, materials, and
personnel in the facility achieve the desired result. This requires verification and routine monitoring
of the process. Likewise, any deviation by the processor from the instructions provided with the
instrument's DFU should be properly evaluated for effectiveness and potential adverse consequences.
Please refer to nationally recognized standards, or to your facility’s standard procedures.

STERILIZER TYPE SAMPLE TEMPERATURE MINIMUM EXPOSURE MINIMUM DRYING

CONFIGURATION TIME (MINUTES) TIME (MINUTES)

Gravity Displacement Wrapped 132 ºC (270 ºF) 15 15

Gravity Displacement Unwrapped 132 ºC (270 ºF) 10 N/A

Pre-vacuum Wrapped 135 ºC (275 ºF) 3 16

Pre-vacuum Unwrapped 132 ºC (270 ºF) 4 N/A

Table 4-1 Sterilization Temperature and Time Settings.

8065751772 4.5
FOR REFERENCE ONLY
FUSE REPLACEMENT

1. Turn the primary AC power switch OFF. It is located at the bottom of the rear
panel on the power module. Unplug power cord from power module.

2. Insert a flat surfaced instrument along the left side of the power module fuse door.
Pressing the flat instrument to the right against the fuse door, pull out to release door.

CAUTION

The fuse door must be pressed gently to ensure it does not break.

3. With fuse door open, grasp the fuse holder and pull it out from the power module.

4. Gently remove and replace fuses. Contact Alcon Technical Services for the correct
rating and size.

5. Reinsert fuse holder into power module and shut the fuse door.
6. Plug power cord into power source.

4.6
FOR REFERENCE ONLY 8065751772
PACKING THE CENTURION® SYSTEM FOR TRANSIT

To avoid damage during transport, careful preparation of the instrument is required

prior to placing it in a vehicle. The display screen and instrument tray must be
properly secured using straps and cushion material. The figure below is an example
of a proper way to secure the display screen and instrument tray (materials from the
original shipping container are used in this example).

Strap secures display

and instrument tray for safe
transport. If desired, one strap
for the display, and one strap
for the instrument tray, can
be used.

Cushion material placed

between display and top
work surface.

Cushion material placed

between instrument tray
and front connector panel.

Figure 4-2 PACKING SYSTEM FOR TRANSIT - This diagram is an example of a

proper way to secure the display screen and instrument tray prior to transportation.

8065751772 4.7
FOR REFERENCE ONLY
SETTING UP THE RECONSTITUTION RACK

The reconstitution rack is used to hold up to six fluid bags for the Active Fluidics™
system, making it convenient for the surgery team to prepare the system for each
surgery. The rack comes in a box that must be opened and set up as instructed below.

STEP ONE: Remove reconstitution rack from shipping box. Discard all shipping
materials (see Figures 4-3A & 4-3B).

STEP TWO: Unfold rack into its standup position and place it on a flat, firm surface
(see Figure 4-3C).

STEP THREE: Hang fluidics bags from plastic tray as shown (see Figure 4-3D).

STEP FOUR: Upon completion of the day's surgery schedule, remove any unused
fluidics bags and store the rack in a safe, clean place.

CAUTION
Prior to using the rack for the first time, clean it in a hot dishwasher. Clean with
an approved disinfecting solution after usage per facility protocol instructions. Do
not attempt to clean this rack in an autoclave.

A B

C D

Figure 4-3 Setting Up the Reconstitution Rack

4.8
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION FIVE
TROUBLESHOOTING

INTRODUCTION

Table 5-1 is a general troubleshooting guide that addresses observations/symptoms and

what the operator can do to try and solve the observed event. Figure 5-4 and Table 5-2
are presented as aids to rapid location of failed or malfunctioning parts or components in
the Centurion® Vision System. In all cases, should the corrective actions not provide the
desired result, call Alcon Technical Services.

For Technical Service contact information open the Custom/About dialog in the
Centurion® Vision System.

System Messages
The system communicates through the display of system messages–Advisories,
Warnings, and Faults–based on the severity of the event. Listed below are examples of
each.

Advisories
An Advisory is a message to the user (see Figure 5-1). The Advisory may require user
intervention, or it may be for information purposes only. When an advisory condition is
detected, the following occurs:
• A tone is generated.
• A dialog is displayed indicating the Advisory.

Figure 5-1 ADVISORIES SCREEN - This is a typical example of an Advisories dialog.

8065751772 5.1
FOR REFERENCE ONLY
 Warnings
Warnings are generated to indicate a non-system fault (see Figure 5-2) that is isolated and
does not affect the whole system. When a Warning is detected, the following occurs:
• A tone is generated.
• A dialog is displayed indicating the Warning.
• Affected mechanisms are placed in a safe state–the function of the affected
mechanism is not available.
• If desired, continue with limited functionality.

Figure 5-2 WARNINGS SCREEN - This is a typical example of a Warnings dialog.

5.2
FOR REFERENCE ONLY 8065751772
 System Faults
System Faults are the result of an exceptional condition resulting from an event or a hardware
issue that renders the software unable to carry out a requested service, or one that results in
unacceptable risk (see Figure 5-3). When a System Fault is detected, the following occurs:
• A tone is generated.
• All mechanisms are disabled.
• A dialog is displayed indicating the fault. If the System Fault occurs during system
initialization, shutdown, or when the touchscreen graphics software is unavailable,
the fault dialog will be displayed in English.
• All requests for functions are ignored, including key activations.

Figure 5-3 FAULTS SCREEN - This is a typical example of a System Fault dialog.

8065751772 5.3
FOR REFERENCE ONLY
 No message is displayed, but Follow the Observed Conditions
unable to setup and operate as table in this section of the operator’s
Event described in this operator's manual manual. If unable to fix the issue, or
Encountered and other applicable labeling. if the symptom is not described in
the observed conditions, contact
Alcon Technical Services.

Advisory XXX
Unit displays an Advisory number Follow the Advisories Troubleshooting
and message. These messages table in this section of the operator’s
are displayed within a dialog box manual. If unable to fix the issue,
and have a green background. write down the Advisory number and
message exactly as it appears on
the screen, then contact Alcon
Technical Services.

Warning XXX
Unit displays a Warning number Write down the Warning number and
and message. These messages message exactly as it appears on the
are displayed within a dialog box screen, then contact Alcon Technical
and have a yellow background. Services. Some or all of the functions
could be disabled. Do not use unit
unless the case is already started
and no back-up is available.

System Fault: XXX

Unit displays a System Fault Write down the Fault number and
number and message. These message exactly as it appears on the
messages are displayed within a screen, then contact Alcon Technical
dialog box and have a red Services. Discontinue use of unit
background. until the problem is resolved.

Figure 5-4 TROUBLESHOOTING GUIDE - When an Event is encountered, refer to this chart first.

5.4
FOR REFERENCE ONLY 8065751772
 OBSERVED CONDITIONS

SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

System does not power-up. 1. Main power switch in OFF position. 1. Turn main power switch near power
cord to ON position.

2. Blown power fuse. 2. Replace power fuse near power cord.

Gravity Fluidics - Test chamber does 1. Restriction to irrigation inflow. 1. Check for kinks in irrigation line or
not fill. There is insufficient irrigation. twisted infusion sleeve.

2. Bottle too low or handpiece too high. 2. Put bottle at 78 cm and put handpiece
at patient eye level.

3. Drip chamber not adequately filled 3. Squeeze drip chamber until 2/3 to
with fluid. 3/4 full.

4. Clogged handpiece or tips. 4. Check handpiece and tips.

5. Faulty FMS. 5. Replace FMS.

Active Fluidics™ System - Test 1. Restriction to irrigation inflow. 1. Check for kinks in irrigation line or
chamber does not fill. There is twisted infusion sleeve.
insufficient irrigation.
2. Clogged handpiece or tips. 2. Check handpiece and tips.

3. FMS. 3. Replace FMS.

Gravity Fluidics - Vacuum check 1. Improper FMS insertion. 1. Reinsert FMS.

failure.
2. IRR and ASP fittings are not con- 2. Ensure both fittings are tightly con-
nected together securely. nected together.

3. Drip chamber not 2/3 to 3/4 full. 3. Flush irrigation line and fill drip cham-
ber halfway using Fill button in Setup
mode. Reprime.

4. Test chamber not on handpiece, or 4. Secure test chamber tightly onto

not secured tightly onto handpiece. handpiece.

5. Priming with HP attached. 5. Remove HP, then connect blue and

white luer fittings together.

6. Cracked blue luer fitting. 6. Check fitting and replace FMS as

necessary.

7. Faulty FMS. 7. Replace FMS.

Active Fluidics™ System - Vacuum 1. Improper FMS insertion. 1. Reinsert FMS.

check failure.
2. IRR and ASP fittings are not con- 2. Ensure both fittings are tightly con-
nected together securely. nected together.

3. Test chamber not on handpiece, or 3. Secure test chamber tightly onto

not secured tightly onto handpiece. handpiece.

4. Priming with HP attached. 4. Remove HP, then connect blue and

white luer fittings together.

5. Cracked blue luer fitting. 5. Check fitting and replace FMS as

necessary.

6. Faulty FMS. 6. Replace FMS.

Table 5-1 OBSERVED CONDITIONS - Listed in this table are observed conditions that may be presented to the
user. The observed Symptom is followed by the Probable Cause and its Corrective Action.

8065751772 5.5
FOR REFERENCE ONLY
 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

Gravity Fluidics - Vent test failure or 1. Restriction in irrigation or aspiration 1. Check kinked irrigation or aspiration
vacuum and vent check failure. lines. lines or twisted tip cap sleeve.

2. Machine insufficiently primed. 2. Press Test to reprime.

3. Faulty FMS. 3. Reinsert FMS. Replace FMS if prob-

lem persists.

Active Fluidics™ System - Vent test 1. Restriction in irrigation or aspiration 1. Check kinked irrigation or aspiration
failure or vacuum and vent check lines. lines or twisted tip cap sleeve.
failure.
2. Machine insufficiently primed. 2. Press Test to reprime.

3. Faulty FMS. 3. Reinsert FMS. Replace FMS if prob-

lem persists.

Prime Complete / Test Handpiece 1. Faulty tip. 1. Remove tip and replace if faulty.
Failed. Retighten. Retest.

2. Faulty handpiece connector. 2. Unplug, reinsert into port, retest.

3. Bad connector port. 3.Connect handpiece to other port and
retune.

4. Faulty handpiece. 4. Replace handpiece. Retest.

5. Other. 5. Record the failed code number and

contact Alcon Technical Services
Department.

Test Handpiece Failed: Loose Tip. 1. Loose tip. 1. Tighten tip and retune.

2. Bad tip. 2. Replace tip and retune.

3. Bad connector port. 3. Connect handpiece to other port and

retune.

Test Handpiece Failed: Tuning in Air. Attempted to tune tips in presence Fill test chamber completely. Retune.
of air.

Gravity Fluidics - Test chamber 1. Clogged handpiece or tips. 1. Check handpiece and tips irrigation
collapses after tuning completed— flow.
does not refill.
2. Restriction to irrigation flow. 2. Check for kinks in irrigation line or
twisted infusion sleeve.

3. Wrong sleeve on tip. 3. Check for proper sleeve and tip size.

Active Fluidics™ System - Test 1. Clogged handpiece or tips. 1. Check handpiece and tips irrigation
chamber collapses after tuning flow.
completed—does not refill.
2. Restriction to irrigation flow. 2. Check for kinks in irrigation line or
twisted infusion sleeve.

3. Wrong sleeve on tip. 3. Check for proper sleeve and tip size.

5.6
FOR REFERENCE ONLY 8065751772
 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

No tune or loss of phaco power. 1. Handpiece tuned while hot. 1. Retune.

2. Loose tip. 2. Retighten and retune.

3. Handpiece connector not seated 3. Disconnect and reinsert handpiece con-

correctly. nector.

4.Bad connector port. 4.Connect handpiece to other port and

retune.

5. Faulty handpiece. 5. Try alternate handpiece.

Gravity Fluidics - Air in irrigation line 1. Drip chamber not sufficiently full. 1. Fill drip chamber 2/3 to 3/4 full.
causing bubbles. Flush irrigation line in Free Flow or
footpedal position 1.

2. Air in line or handpiece. 2. Tap handpiece 2-3X during flow test.

3. Loose irrigation luer fitting. 3. Check irrigation line and reseat.

4. Improper priming. 4. Reprime per setup procedure.

5. Bad handpiece. 5. Replace handpiece.

Active Fluidics™ System - Air in 1. Air in line or handpiece. 1. Tap handpiece 2-3X during flow test.
irrigation line causing bubbles.
2. Loose irrigation luer fitting. 2. Check irrigation line and reseat.

3. Improper priming. 3. Reprime per setup procedure.

4. Bad handpiece. 4.Replace handpiece.

Irrigation does not stop. System in Continuous Irrigation mode. Turn Continuous Irrigation off.

Low irrigation flow. Irrigation sleeve too distal. Move sleeve so holes are proximal to
tip flare.

Backflow regurgitation. Machine insufficiently primed. Reprime.

Insufficient aspiration. 1. Loose blue luer fittings. 1. Reconnect securely.

2. Damaged O‑ring (Ultraflow® I/A hand- 2. Inspect O‑ring and replace, as neces-
piece only). sary.

3. Clogged tip. 3. • Flush tip with sterile water or BSS®

sterile irrigating solution. Retest.
• Replace tip. Retest.

4. Kinked or damaged tubing. 4. Check tubing and/or replace FMS.

5. Cracked blue luer fitting. 5. Check fitting and/or replace FMS.

Ultraflow™* I/A handpiece leaking at 1. Loose tip. 1. Retighten tip.

tip and handpiece connection.
2. Damaged O‑ring. 2. Retest. Inspect O‑rings and replace,
as neces­sary. To replace:
• Using the special O‑ring tool, re-
move damaged O‑ring.
• Roll new O‑ring off tool and roll it
into place on tip.

3. Leak in tubing. 3. Replace tubing.

8065751772 5.7
FOR REFERENCE ONLY
 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

“Calibration failed. Vitrectomy cut rate Internal pneumatics valve calibration Continue vitrectomy procedure with lim-
will be limited to 800 cpm” Advisory is has failed. ited cut rate and contact Alcon Technical
displayed at power up. Services Department.

Ineffective or poor Vit cutting. 1. Port not closing fully as the inner 1. Reduce cutting speed until port
cutter moves. closes completely.

2. Kinked, damaged or loose actuation 2. Check for damaged or kinked tubing;

tubing. straighten if necessary. Tighten any
loose luer fittings. Replace probe if
visual inspection shows any dam-
aged components.

3. Faulty probe (activated in air instead 3. Replace probe.

of fluid).

Ant Vit probe does not work at all (no 1. An actuation line filling with BSS® 1. Check for correct tubing connections,
movement). fluid due to improper setup. then replace probe.

2. Faulty probe. 2. Replace probe.

Gravity Fluidics - IV pole does not System error. Turn system on, wait until system
retract completely upon shutdown. powers up, then turn system off using
Standby power switch located on upper
rear panel.

Remote control does not work. 1. Remote control and system set on 1. Verify system channel selection and
different channels. remote channel select are set to same
channel (A, B, C, D, E, or F).

2. Batteries discharged. 2. Replace batteries in remote control.

Cabled Footswitch - Footpedal not 1. Footpedal was pressed when system 1. Release footpedal and power off
responding properly. was powered up, or footpedal was system. Make sure footswitch is
pressed while plugging in footswitch. properly connected to system, and
turn power back on, with footpedal
in full up position.

2. Footswitch connector not seated 2. Disconnect and reconnect footswitch

properly. cable connector.

3. Debris or BSS® solution residue 3. Clean and remove debris.

under rear section of treadle.

4. Console malfunction. 4. Disconnect and reconnect footswitch

cable connector.

5. Faulty footswitch. 5. Replace footswitch.

Wireless Footswitch - Footpedal not 1. Footpedal was pressed down when 1. Release footpedal and power off
responding properly. system was powered up system. Turn power back on, with
footpedal in full up position.

2. Debris or BSS® solution residue 2. Clean and remove debris.

under rear section of treadle.

3. Wireless communications not work- 3. Connect footswitch to console with

ing properly. cable.

4. Faulty footswitch. 4. Replace footswitch.

5.8
FOR REFERENCE ONLY 8065751772
 SYMPTOM PROBABLE CAUSE CORRECTIVE ACTION

Cabled Footswitch - “Please Install 1. Improperly connected or discon- 1. Verify proper insertion of footswitch
Footswitch” Advisory is displayed. nected footswitch. cable connector (while footpedal/
treadle is in full up position).

2. Footswitch connector not seated 2. Disconnect and reconnect footswitch

properly. cable connector.

3. Faulty footswitch. 3. Replace footswitch.

Wireless Footswitch - “Please Install 1. Footswitch has not been “paired” with 1. Hang footswitch onto footswitch
Footswitch” Advisory is displayed. the console. hooks on the rear of the unit for
greater than 5 seconds then remove.

System Fault occurs; entire system System Fault has several possible Carefully record all text appearing in
inoperative, red screen with stop sign causes. Fault screen, on display. Press and hold
is displayed. Standby switch for a few seconds to turn
system off, wait until screen goes dark,
then turn system back on to see whether
fault clears. Contact Technical Services.

“Doctor data invalid, U/S Occlusion, Dr. User restores, or selects Doctor Name Save data. U/S Occlusion settings will
XXXX” Advisory is displayed. that contains U/S Occlusion settings be removed.
which are no longer available.

8065751772 5.9
FOR REFERENCE ONLY
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED

100 - Fluidics Mechanism 157 Advisory xxx

Active Fluidics is not available.
101-149 Warning xxx Recommended actions:
Fluidics not available. 1) Remove FMS.
Recommended actions: 2) Use Gravity Fluidics.
1) If in surgery, stabilize the eye then restart 3) If condition persists, note Advisory number
system. and contact Alcon Technical Services.
2) If condition persists after restart, note See the About Dialog for Alcon Technical
Warning number and contact Alcon Technical Services contact information.
Services.
See the About Dialog for Alcon Technical 158 Advisory xxx
Services contact information. Aspiration, phaco power, and vitrectomy cutting
are unavailable.
150 Advisory xxx Recommended actions:
Irrigation bag empty. 1) Check for irrigation path obstructions.
Recommended actions: 2) Replace FMS.
1) Release footswitch treadle. 3) If condition persists, note Advisory number
2) Remove handpiece from eye. and contact Alcon Technical Services.
3) Replace bag. See the About Dialog for Alcon Technical
Services contact information.
151 Advisory xxx
Irrigation bag empty. 159 Advisory xxx
Recommended actions: Irrigation is unavailable.
1) Replace bag. Recommended actions:
1) Replace FMS.
153 Advisory xxx 2) If condition persists, note Advisory number
Bag bay door open. and contact Alcon Technical Services.
Recommended actions: See the About Dialog for Alcon Technical
1) Close door. Services contact information.
2) Proceed with surgery.
Alternate actions: 160 Advisory xxx
1) Remove handpiece from eye. FMS calibration failed.
2) Press ‘Return to Setup Screen’. Recommended actions:
1) Reinsert FMS.
154 Advisory xxx 2) If condition persists, replace FMS.
Bag bay door was opened.
Recommended actions: 161-167 Advisory xxx
1) Close bag door. Vacuum check failed.
2) Repeat operation. Recommended actions:
1) Check luer fittings and reprime.
155 Advisory xxx 2) If condition persists, reinsert or replace FMS.
Irrigation bag is almost empty. 3) If condition persists, note Advisory number
Recommended actions: and contact Alcon Technical Services.
1) Replace bag. See the About Dialog for Alcon Technical
Services contact information.
156 Advisory xxx
Active Fluidics is not available. 168 Advisory xxx
Recommended actions: Flow obstruction.
1) Remove FMS. Recommended actions:
2) Use Gravity Fluidics. 1) Check handpiece free flow.
3) If condition persists, note Advisory number 2) If condition persists, replace phaco tip or
and contact Alcon Technical Services. sleeve.
See the About Dialog for Alcon Technical 3) If condition persists, note Advisory number
Services contact information. and contact Alcon Technical Services.
See the About Dialog for Alcon Technical
Services contact information.

Table 5-2 EVENT CODES - Listed in this table are messages shown on the Centurion® Vision System
display panel when the system detects an event. The Event codes are separated between
Advisories, Warnings, and Faults.

5.10
FOR REFERENCE ONLY 8065751772
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
169 Advisory xxx 191 Advisory xxx
Irrigation pressure is low. Active Fluidics is not available.
Recommended actions: Recommended actions:
1) Check bottle fluid level. 1) Remove FMS.
Alternate actions: 2) Use Gravity Fluidics.
1) Check for kinked lines or loose fittings. 3) If condition persists, note Advisory number
and contact Alcon Technical Services.
170 Advisory xxx See the About Dialog for Alcon Technical
Reflux terminated. Reflux fluid volume depleted. Services contact information.
Reflux will be unavailable until fluid is aspirated.
Recommended actions: 200 - Ultrasonics Mechanism
1) Aspirate fluid.
201-249 Warning xxx
171 Advisory xxx Ultrasound not available.
Drain bag is full. Recommended actions:
Recommended actions: 1) If in surgery, stabilize the eye then restart
1) Replace FMS. system.
2) If condition persists after restart, note
179 Advisory xxx Warning number and contact Alcon Technical
FMS barcode invalid. Services.
Recommended actions: See the About Dialog for Alcon Technical
1) Reinsert FMS Services contact information.
2) If condition persists, replace FMS.
250 Advisory xxx
180 Advisory xxx Testing in air.
Invalid FMS ID. Recommended actions:
Recommended actions: 1) Fill test chamber completely.
1) Reinsert FMS. 2) Re-test handpiece.
2) If condition persists, replace FMS. Alternate actions:
1) Connect handpiece to other port and re-test.
181 Advisory xxx 2) If condition persists, replace handpiece.
FMS calibration failed. 3) If condition persists, note Advisory number
Recommended actions: and contact Alcon Technical Services.
1) Reinsert FMS. See the About Dialog for Alcon Technical
2) If condition persists, replace FMS. Services contact information.
3) If condition persists, restart system.
4) If condition persists, note Advisory number 254-255 Advisory xxx
and contact Alcon Technical Services. Loose tip.
See the About Dialog for Alcon Technical Recommended actions:
Services contact information. 1) Tighten or replace tip.
2) Re-test handpiece.
182 Advisory xxx Alternate actions:
FMS calibration failed. 1) Connect handpiece to other port.
Recommended actions: 2) Re-test handpiece.
1) Reinsert FMS. 3) If condition persists, replace handpiece.
2) If condition persists, replace FMS.
3) If condition persists, restart system. 256-266 Advisory xxx
4) If condition persists, note Advisory number Handpiece test failed.
and contact Alcon Technical Services. Recommended actions:
See the About Dialog for Alcon Technical 1) Remove and reconnect handpiece.
Services contact information. 2) If condition persists, try other port.
3) If condition persists, replace handpiece.
190 Advisory xxx 4) If condition persists and in surgery, stabilize
Active Fluidics is not available. the eye then restart system.
Recommended actions: 5) If condition persists after restart, note
1) Remove FMS. Advisory number and contact Alcon Technical
2) Use Gravity Fluidics. Services.
3) If condition persists, note Advisory number See the About Dialog for Alcon Technical
and contact Alcon Technical Services. Services contact information.
See the About Dialog for Alcon Technical
Services contact information. 268 Advisory xxx
Handpiece test failed.
Recommended actions:
1) Press ‘Return to Setup Screen’.
2) Re-test handpiece.

8065751772 5.11
FOR REFERENCE ONLY
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
269 Advisory xxx 290 Advisory xxx
Handpiece test failed. Ultrasound error.
Recommended actions: Recommended actions:
1) Re-test handpiece. 1) Release footswitch treadle and retry.
2) If condition persists and in surgery, stabilize
270-273 Advisory xxx the eye then restart system.
Handpiece fault detected. 3) If condition persists after restart, note
Recommended actions: Advisory number and contact Alcon
1) Connect handpiece to other port. Technical Services.
2) Re-test handpiece. See the About Dialog for Alcon Technical
3) If condition persists, replace handpiece. Services contact information.
4) If condition persists and in surgery, stabilize
the eye then restart system. 291 Advisory xxx
5) If condition persists after restart, note Ultrasound error.
Advisory number and contact Alcon Technical Recommended actions:
Services. 1) Release footswitch treadle, wait 10 seconds,
See the About Dialog for Alcon Technical then retry.
Services contact information. 2) If condition persists and in surgery, stabilize
the eye then restart system.
274 Advisory xxx 3) If condition persists after restart, note
Ultrasound error. Advisory number and contact Alcon
Recommended actions: Technical Services.
1) Release footswitch treadle and retry. See the About Dialog for Alcon Technical
2) If condition persists and in surgery, stabilize Services contact information.
the eye then restart system.
3) If condition persists after restart, note 293 Advisory xxx
Advisory number and contact Alcon Technical Ultrasound error.
Services. Recommended actions:
See the About Dialog for Alcon Technical 1) Release footswitch treadle and retry.
Services contact information. 2) If condition persists and in surgery, stabilize
the eye then restart system.
277 Advisory xxx 3) If condition persists after restart, note
Handpiece disconnected while applying U/S Advisory number and contact Alcon
power. Technical Services.
Recommended actions: See the About Dialog for Alcon Technical
1) Release footswitch treadle. Services contact information.
2) Insert and test handpiece.

278 Advisory xxx 300 - Footswitch Mechanism

Handpiece fault detected.
Recommended actions: 301-349 Warning xxx
1) Connect handpiece to other port. Surgical functionality not available.
2) Re-test handpiece. Recommended actions:
3) If condition persists, replace handpiece. 1) If in surgery, stabilize the eye then restart
4) If condition persists and in surgery, stabilize system.
the eye then restart system. 2) If condition persists after restart, note
5) If condition persists after restart, note Warning number and contact Alcon Technical
Advisory number and contact Alcon Technical Services.
Services. See the About Dialog for Alcon Technical
See the About Dialog for Alcon Technical Services contact information.
Services contact information.
350 Advisory xxx
279-280 Advisory xxx Footswitch failure detected.
Unknown handpiece detected. Recommended actions:
Recommended actions: 1) Inspect footswitch, clean under rear
1) Remove and inspect cable connector for section of treadle and remove debris if
debris. present. (Reference Maintenance section
2) Verify handpiece compatibility. of Operator’s Manual.)
3) If condition persists, connect to other port. 2) Inspect and reconnect footswitch connector.
4) If condition persists, replace handpiece. 3) Ensure treadle is not depressed then reset
5) If condition persists and in surgery, stabilize footswitch.
the eye then restart system. 4) If condition persists, replace footswitch.
6) If condition persists after restart, note Advisory 5) If condition persists, note Advisory number
number and contact Alcon Technical Services. and contact Alcon Technical Services.
See the About Dialog for Alcon Technical See the About Dialog for Alcon Technical
Services contact information. Services contact information.

5.12
FOR REFERENCE ONLY 8065751772
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
351 Advisory xxx 363 Advisory xxx
Footswitch failure detected. Footswitch communication lost.
Recommended actions: Recommended actions:
1) Inspect and reset footswitch. 1) Release footswitch treadle.
2) If condition persists, replace footswitch. 2) If footswitch is wireless, move footswitch and
3) If condition persists, note Advisory number console closer, or eliminate obstruction.
and contact Alcon Technical Services. 3) If footswitch is cabled, replace cable.
See the About Dialog for Alcon Technical 4) If condition persists, replace footswitch.
Services contact information.
364-365 Advisory xxx
352 Advisory xxx Footswitch failure detected.
Footswitch failure. Recommended actions:
Recommended actions: 1) Release footswitch treadle.
1) Inspect and reconnect footswitch connector. 2) If condition persists, replace footswitch.
2) If condition persists, replace footswitch.
3) If condition persists, note Advisory number 366 Advisory xxx
and contact Alcon Technical Services. Footswitch detent failure detected. Detent
See the About Dialog for Alcon Technical vibration will not be provided.
Services contact information. Recommended actions:
1) Release footswitch treadle.
358-359 Advisory xxx 2) Proceed with surgery.
Footswitch charging while cradled is unavailable. 3) If condition persists after restart, replace
Recommended actions: footswitch.
1) Cable the footswitch if charging is desired.
2) If condition persists after restart, note 367-368 Advisory xxx
Advisory number and contact Alcon Technical Footswitch failure detected.
Services. Recommended actions:
See the About Dialog for Alcon Technical 1) Release footswitch treadle.
Services contact information. 2) If condition persists, replace footswitch.

360 Advisory xxx 369 Advisory xxx

Footswitch battery is low. Footswitch wireless operation unavailable.
Recommended actions: Recommended actions:
1) Cradle the footswitch after surgical cases 1) Do not disconnect footswitch cable.
have been completed. 2) If condition persists, replace footswitch.
2) If condition persists, note Advisory number
and contact Alcon Technical Services. 370 Advisory xxx
See the About Dialog for Alcon Technical Footswitch failure detected.
Services contact information. Recommended actions:
1) Release footswitch treadle.
361 Advisory xxx 2) If condition persists, replace footswitch.
Footswitch battery is critically low. Footswitch
functionality may be lost unexpectedly. 371 Advisory xxx
Recommended actions: Footswitch failure detected.
1) Connect footswitch cable to console. Recommended actions:
2) Cradle the footswitch after surgical cases 1) Release footswitch treadle.
have been completed. 2) If condition persists, replace footswitch.
3) If condition persists, note Advisory number
and contact Alcon Technical Services. 372-376 Advisory xxx
See the About Dialog for Alcon Technical Footswitch failure detected.
Services contact information. Recommended actions:
1) Release footswitch treadle and buttons.
362 Advisory xxx 2) Place footswitch in horizontal position.
Footswitch version not supported. 3) If condition persists, replace footswitch.
Recommended actions:
1) Replace footswitch. 377-380 Advisory xxx
2) If condition persists, note Advisory and Footswitch failure detected.
contact Alcon Technical Services. Recommended actions:
See the About Dialog for Alcon Technical 1) Release footswitch treadle.
Services contact information. 2) If condition persists, replace footswitch.

381-382 Advisory xxx

Footswitch failure detected.
Recommended actions:
1) Connect footswitch cable to console.
2) If condition persists, replace footswitch.

8065751772 5.13
FOR REFERENCE ONLY
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
383 Advisory xxx 451 Advisory xxx
Footswitch pairing failed. Wireless operation Cannot recognize footswitch.
unavailable. Recommended actions:
Recommended actions: 1) Check footswitch connection and reset
1) Remove and re-cradle the footswitch for at footswitch.
least 5 seconds. 2) If condition persists, note Advisory number
Alternate actions: and contact Alcon Technical Services.
1) Connect footswitch cable to console. See the About Dialog for Alcon Technical
2) If condition persists, replace footswitch. Services contact information.

387-388 Advisory xxx 452 Advisory xxx

Footswitch wireless operation unavailable. The IOP setting cannot be achieved due to the
Recommended actions: current PEL setting. The IOP setting will be
1) If in surgery, do not disconnect footswitch adjusted to the closest valid setting.
cable. Recommended actions:
2) Between surgical cases, disconnect and 1) Note current IOP and PEL settings.
reconnect footswitch cable. 2) Update settings as necessary or proceed
3) If condition persists, replace footswitch. with current settings.

453 Advisory xxx

400 - Host The Irrigation Pressure setting cannot be
achieved due to the current PEL setting. The
400-420 Fault xxx Irrigation Pressure setting will be adjusted to
System not operational. the closest valid setting.
Recommended actions: Recommended actions:
1) Press Standby Switch to shut down system. 1) Note current Irrigation Pressure and PEL
2) Restart system. settings.
3) If condition persists, note Fault number and 2) Update settings as necessary or proceed
contact Alcon Technical Services. with current settings.
See the About Dialog for Alcon Technical
Services contact information. 460 Advisory xxx
Footswitch not detected.
431 Warning xxx Recommended actions:
AC power lost. Continuing on battery power. 1) Install footswitch.
Surgical functionality is not available.
Recommended actions: 463 Advisory xxx
1) Restore AC power as soon as possible to The language translation is invalid.
reactivate surgical functionality. Recommended actions:
1) Proceed with surgical cases.
432 Warning xxx 2) Note Advisory number and contact Alcon
Backup power depleted. System will shut down. Technical Services.
Recommended actions: See the About Dialog for Alcon Technical
1) If in surgery, stabilize the eye then restore Services contact information.
AC power and restart system.
464 Advisory xxx
433 Warning xxx The selected language translation is invalid.
Backup power unavailable. System will shut English will be used by default.
down. Recommended actions:
Recommended actions: 1) Proceed with surgical cases.
1) If in surgery, stabilize the eye then restore 2) Note Advisory number and contact Alcon
AC power and restart system. Technical Services.
See the About Dialog for Alcon Technical
450 Advisory xxx Services contact information.
Footswitch is depressed.
Recommended actions: 465 Advisory xxx
1) Release footswitch treadle before pressing The test sequence was interrupted by removal
Prime FMS, Fill, or Test Handpiece. of the handpiece.
2) If condition persists, clear obstruction Recommended actions:
preventing footswitch release. 1) Install handpiece and re-test.

466 Advisory xxx

A third handpiece has been inserted. This
handpiece has been disabled.
Recommended actions:
1) Remove any handpiece.

5.14
FOR REFERENCE ONLY 8065751772
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
468 Advisory xxx 486 Advisory xxx
Doctor file unavailable. The AutoSert setup operation was canceled due
Recommended actions: to a step change.
1) Restore doctor file from backup media. Recommended actions:
2) If condition persists, note Advisory number 1) Select an I/A or AutoSert step.
and contact Alcon Technical Services. 2) Continue AutoSert handpiece setup.
Alternate actions:
1) Select Alcon Settings doctor file. 491 Advisory xxx
See the About Dialog for Alcon Technical Wi-Fi network initialization failed. Wireless
Services contact information. Video Overlay is not available.
Recommended actions:
469 Advisory xxx 1) You may proceed with surgical cases.
Doctor file corrupted. 2) Optionally, you may restart the system to
Recommended actions: correct the condition.
1) Restore doctor file from backup media. 3) If condition persists after restart, note
2) If condition persists, note Advisory number Advisory number and contact Alcon Technical
and contact Alcon Technical Services. Services.
Alternate actions: See the About Dialog for Alcon Technical
1) Select Alcon Settings doctor file. Services contact information.
See the About Dialog for Alcon Technical
Services contact information.
500 - Vit Mechanism
470 Advisory xxx
Doctor file invalid. 501-549 Warning xxx
Recommended actions: Vitrectomy not available.
1) Restore doctor file from backup media. Recommended actions:
2) If condition persists, note Advisory number 1) If in surgery, stabilize the eye then restart
and contact Alcon Technical Services. system.
Alternate actions: 2) If condition persists after restart, note
1) Select Alcon Settings doctor file. Warning number and contact Alcon Technical
See the About Dialog for Alcon Technical Services.
Services contact information. See the About Dialog for Alcon Technical
Services contact information.
473 Advisory xxx
System service needed. 550 Advisory xxx
Recommended actions: Vitrectomy high-speed cutting is compromised.
1) Note Advisory number. Recommended actions:
2) Proceed with surgical cases. 1) Proceed with lower cut rate 2000 cpm or
3) Contact Alcon Technical Services for system below, or replace vitrector.
service. 2) If condition persists, note Advisory number
See the About Dialog for Alcon Technical and contact Alcon Technical Services.
Services contact information. See the About Dialog for Alcon Technical
Services contact information.
475 Advisory xxx
CPU Battery should be replaced. System clock 551 Advisory xxx
may be incorrect. Vitrectomy cutting is disabled.
Recommended actions: Recommended actions:
1) Note Advisory number. 1) Check vitrector connection.
2) Update date and time. 2) If condition persists, note Advisory number
3) Proceed with surgical cases. and contact Alcon Technical Services.
4) Contact Alcon Technical Services to replace See the About Dialog for Alcon Technical
battery. Services contact information.
See the About Dialog for Alcon Technical
Services contact information. 552 Advisory xxx
Vitrectomy cutting is unavailable.
477 Advisory xxx Recommended actions:
System security has been compromised. 1) Release footswitch treadle.
Recommended actions: 2) Check vitrector connection.
1) Note Advisory number. 3) If condition persists and in surgery, stabilize
2) Contact Alcon Technical Services. the eye then restart system.
See the About Dialog for Alcon Technical 4) If condition persists, note Advisory number
Services contact information. and contact Alcon Technical Services.
See the About Dialog for Alcon Technical
Services contact information.

8065751772 5.15
FOR REFERENCE ONLY
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
600 - Coag Mechanism 860 Advisory xxx
Two AutoSert Handpieces detected.
601-649 Warning xxx Recommended actions:
Coagulation is not available. 1) Remove one AutoSert Handpiece and
Recommended actions: proceed.
1) If in surgery, stabilize the eye then restart
system. 888 Advisory xxx
2) If condition persists after restart, note AutoSert error occurred.
Warning number and contact Alcon Technical Recommended actions:
Services. 1) Retry AutoSert operation.
See the About Dialog for Alcon Technical 2) If condition persists, replace AutoSert
Services contact information. Handpiece.
3) If condition persists and in surgery, stabilize
650 Advisory xxx the eye then restart system.
Coagulation is not available. 4) If condition persists after restart, note
Recommended actions: Advisory number and contact Alcon Technical
1) If condition persists and in surgery, stabilize Services.
the eye then restart system. See the About Dialog for Alcon Technical
2) If condition persists, note Advisory number Services contact information.
and contact Alcon Technical Services.
See the About Dialog for Alcon Technical 889 Advisory xxx
Services contact information. Handpiece fault detected.
Recommended actions:
1) Replace AutoSert handpiece.
700 - IV Pole Mechanism 2) If condition persists and in surgery, stabilize
the eye then restart system.
701-749 Warning xxx 3) If condition persists after restart, note
IV Pole not available. Advisory number and contact Alcon Technical
Recommended actions: Services.
1) If in surgery, stabilize the eye then restart See the About Dialog for Alcon Technical
system. Services contact information.
2) If condition persists after restart, note
Warning number and contact Alcon Technical 890 Advisory xxx
Services. AutoSert error occurred.
See the About Dialog for Alcon Technical Recommended actions:
Services contact information. 1) Release footswitch treadle and retry.
2) If condition persists, replace AutoSert
750 Advisory xxx handpiece.
IV Pole jammed. Pole may not have achieved 3) If condition persists and in surgery, stabilize
desired height. the eye then restart system.
Recommended actions: 4) If condition persists after restart, note
1) Check for external obstacles. Advisory number and contact Alcon Technical
2) If condition persists and in surgery, stabilize Services.
the eye then restart system. See the About Dialog for Alcon Technical
3) If condition persists, note advisory number Services contact information.
and contact Alcon Technical Services.
See the About Dialog for Alcon Technical 891 Advisory xxx
Services contact information. AutoSert handpiece impeded.
Recommended actions:
1) Release footswitch treadle and retry.
800 - IOL Mechanism 2) If condition persists, replace AutoSert
handpiece.
801-849 Warning xxx 3) If condition persists and in surgery, stabilize
AutoSert not available. the eye then restart system.
Recommended actions: 4) If condition persists after restart, note
1) If in surgery, stabilize the eye then restart Advisory number and contact Alcon Technical
system. Services.
2) If condition persists after restart, note See the About Dialog for Alcon Technical
Warning number and contact Alcon Technical Services contact information.
Services.
See the About Dialog for Alcon Technical
Services contact information.

5.16
FOR REFERENCE ONLY 8065751772
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
892 Advisory xxx 900 - Pump Mechanism
Handpiece fault detected.
Recommended actions: 901-949 Warning xxx
1) Reinsert handpiece cable connector. Vitrectomy not available.
2) If condition persists, replace AutoSert Recommended actions:
Handpiece. 1) If in surgery, stabilize the eye then restart
3) If condition persists and in surgery, stabilize system.
the eye then restart system. 2) If condition persists after restart, note
4) If condition persists after restart, note Warning number and contact Alcon Technical
Advisory number and contact Alcon Technical Services.
Services. See the About Dialog for Alcon Technical
See the About Dialog for Alcon Technical Services contact information.
Services contact information.
950 Advisory xxx
893 Advisory xxx Pump leak detected. Vitrectomy cutting may
AutoSert handpiece calibration failed. be unavailable.
Recommended actions: Recommended actions:
1) Replace AutoSert Handpiece. 1) Verify if vitrectomy cutter is disabled.
2) If condition persists and in surgery, stabilize 2) If condition persists, note advisory number
the eye then restart system. and contact Alcon Technical Services.
3) If condition persists after restart, note See the About Dialog for Alcon Technical
Advisory number and contact Alcon Technical Services contact information.
Services.
See the About Dialog for Alcon Technical
Services contact information. 1000 - AutoCap Mechanism

894 Advisory xxx 1001-1049 Warning xxx

Handpiece must be in fully retracted position Capsulotomy is not available.
prior to autoclave. Recommended actions:
Recommended actions: 1) If in surgery, stabilize the eye then restart
1) Reinsert AutoSert Handpiece. system.
2) If condition persists after restart, note
895 Advisory xxx Warning number and contact Alcon Technical
Handpiece fault detected. Services.
Recommended actions: See the About Dialog for Alcon Technical
1) Replace AutoSert Handpiece. Services contact information.
2) If condition persists and in surgery, stabilize
the eye then restart system. 1050 Advisory xxx
3) If condition persists after restart, note Footswitch is depressed.
Advisory number and contact Alcon Technical Recommended actions:
Services. 1) Release footswitch treadle before enabling
See the About Dialog for Alcon Technical Capsulotomy.
Services contact information.
1061 Advisory xxx
897 Advisory xxx ICD test failed.
Handpiece fault detected. Recommended actions:
Recommended actions: 1) Re-test ICD.
1) Replace AutoSert Handpiece.
2) If condition persists and in surgery, stabilize 1062-1064 Advisory xxx
the eye then restart system. ICD test failed.
3) If condition persists after restart, note Recommended actions:
Advisory number and contact Alcon Technical 1) Remove and reconnect ICD, then re-test
Services. ICD.
See the About Dialog for Alcon Technical 2) If condition persists, replace ICD.
Services contact information. 3) If condition persists and in surgery, stabilize
the eye then restart system.
4) If condition persists after restart, note
Advisory number and contact Alcon Technical
Services.
See the About Dialog for Alcon Technical
Services contact information.

8065751772 5.17
FOR REFERENCE ONLY
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
1065 Advisory xxx 1153-1156 Advisory xxx
ICD test failed. Backup power unavailable. System will shut
Recommended actions: down immediately if AC Power is lost.
1) Press ‘Return to Setup Screen’. Recommended actions:
2) Re-test ICD. 1) You may proceed with surgery.
2) If condition persists, note Advisory number
1072-1076 Advisory xxx and contact Alcon Technical Services.
ICD failed. See the About Dialog for Alcon Technical
Recommended actions: Services contact information.
1) Press ‘Return to Setup Screen’.
2) Remove and reconnect ICD, then re-test
ICD. 1200 - Wireless Mechanism
3) If condition persists, replace ICD.
4) If condition persists and in surgery, stabilize 1201-1249 Warning xxx
the eye then restart system. Wireless features not available.
5) If condition persists after restart, note 1) If in surgery, stabilize the eye then restart
Advisory number and contact Alcon Technical system.
Services. 2) If condition persists after restart, note
See the About Dialog for Alcon Technical Warning number and contact Alcon Technical
Services contact information. Services.
See the About Dialog for Alcon Technical
1099 Capsulotomy is not supported. Services contact information.
Recommended actions:
1) Select a different procedure or remove the 1250 Advisory xxx
Capsulotomy step. Wireless channel is already in use by another
Centurion console.
Recommended actions:
1100 - Power Control Mechanism 1) Open the System Settings dialog and change
the Wireless Channel.
1101-1149 Warning xxx
Mechanism power control error.
Recommended actions: 1300 - Tone Mechanism
1) If in surgery, stabilize the eye.
2) Press Standby Switch for 5 seconds to 1301-1349 Warning xxx
shutdown system. Fluidics and Coagulation not available.
3) Restart system. Recommended actions:
4) If condition persists, note Warning number 1) If in surgery, stabilize the eye then restart
and contact Alcon Technical Services. system.
See the About Dialog for Alcon Technical 2) If condition persists after restart, note
Services contact information. Warning number and contact Alcon Technical
Services.
1150 Advisory xxx See the About Dialog for Alcon Technical
Backup power service needed. System will shut Services contact information.
down immediately if AC Power is lost.
Recommended actions:
1) You may proceed with surgery. 1400 - Operator Control Mechanism
2) If condition persists, note Advisory number
and contact Alcon Technical Services. 1401-1449 Warning xxx
See the About Dialog for Alcon Technical Fluidics not available.
Services contact information. Recommended actions:
1) If in surgery, stabilize the eye then restart
1151 Advisory xxx system.
Backup power temporarily unavailable. Battery is 2) If condition persists after restart, note
recharging. System will shut down immediately Warning number and contact Alcon Technical
if AC Power is lost. Services.
Recommended actions: See the About Dialog for Alcon Technical
1) You may proceed with surgery. Services contact information.
2) If condition persists, note Advisory number
and contact Alcon Technical Services.
See the About Dialog for Alcon Technical
Services contact information.

5.18
FOR REFERENCE ONLY 8065751772
 ADVISORIES

EVENT EVENT
CODE MESSAGE DISPLAYED CODE MESSAGE DISPLAYED
2000 - IA Subsystem 2215 Warning xxx
Footswitch, IV Pole, Pump, Audio, and Operator
2000-2006 Warning xxx Control not available.
Fluidics, Vitrectomy, and Coagulation not Recommended actions:
available. 1) Restart system.
Recommended actions: 2) If condition persists after restart, note
1) If in surgery, stabilize the eye then restart Warning number and contact Alcon Technical
system. Services.
2) If condition persists after restart, note See the About Dialog for Alcon Technical
Warning number and contact Alcon Technical Services contact information.
Services.
See the About Dialog for Alcon Technical
Services contact information.

2015 Warning xxx

Fluidics, Vitrectomy, and Coagulation not
available.
Recommended actions:
1) Restart system.
2) If condition persists after restart, note
Warning number and contact Alcon Technical
Services.
See the About Dialog for Alcon Technical
Services contact information.

2100 - Generator Subsystem

2100-2106 Ultrasonics, Capsulotomy, and AutoSert not

available.
Recommended actions:
1) If in surgery, stabilize the eye then restart
system.
2) If condition persists after restart, note
Warning number and contact Alcon Technical
Services.
See the About Dialog for Alcon Technical
Services contact information.

2115 Warning xxx

Ultrasonics, Capsulotomy, and AutoSert not
available.
Recommended actions:
1) Restart system.
2) If condition persists after restart, note
Warning number and contact Alcon Technical
Services.
See the About Dialog for Alcon Technical
Services contact information.

2200 - Multifunction Subsystem

2200-2206 Warning xxx

Footswitch, IV Pole, Pump, Audio, and Operator
Control not available.
Recommended actions:
1) If in surgery, stabilize the eye then restart
system.
2) If condition persists after restart, note
Warning number and contact Alcon Technical
Services.
See the About Dialog for Alcon Technical
Services contact information.

8065751772 5.19
FOR REFERENCE ONLY
 THIS PAGE INTENTIONALLY BLANK

5.20
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION SIX
ACCESSORIES AND PARTS

In this section of the Centurion® Operator's Manual is a list of accessories, replacement items, and
parts approved by Alcon. Use of non‑approved accessories cannot be permitted.

Please contact the Alcon Sales Department for in-service information prior to initial use of
handpieces, accessories, or packs.

For additional information, please contact the Alcon Sales Department.

Phone: Write:
(800) 862‑5266 or Alcon, Inc.
(817) 293‑0450 6201 South Freeway
Ask for Customer Service Fort Worth, TX. 76134‑2099

INTERNATIONAL: Please contact your local Alcon Sales Office.

8065751772 6.1
FOR REFERENCE ONLY
 DESCRIPTION CATALOG NUMBER

Accessories
CENTURION® OZil® Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751761
OZil® Torsional Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750469
AutoSert® INTREPID® IOL Injector (with plunger and wrench). . . . . . . . . . . . . . 8065751755
Plunger, IOL Injector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751776
Wrench, IOL Injector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751775
Remote Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751774
Footswitch, Centurion® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751762
Footswitch, Centurion® Wired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752572
Footswitch, Constellation® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750977
Operator’s Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751772
Dust Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751773
Centurion® Media Stick. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751771
Centurion® Tray Arm Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752229
Reconstitution Rack. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752527

CENTURION® FMS Packs for Active Fluidics™ Technology, 0.9 mm

Active FMS Pack, Basic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752180
Active FMS Pack, 0.9 mm Tipless. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752181
Active FMS Pack, 0.9 mm INTREPID® Ultra Tipless . . . . . . . . . . . . . . . . . . . 8065752182
Active FMS Pack, 0.9 mm INTREPID® Nano Tipless. . . . . . . . . . . . . . . . . . . 8065752183
Active FMS Pack, 0.9 mm ABS® 30° Kelman®. . . . . . . . . . . . . . . . . . . . . . . 8065752184
Active FMS Pack, 0.9 mm ABS® 45° Kelman®. . . . . . . . . . . . . . . . . . . . . . . 8065752185
Active FMS Pack, 0.9 mm Tapered ABS® 30° Kelman®. . . . . . . . . . . . . . . . . . 8065752186
Active FMS Pack, 0.9 mm Tapered ABS® 45° Kelman®. . . . . . . . . . . . . . . . . . 8065752187
Active FMS Pack, 0.9 mm Mini-Flared ABS® 30° Kelman® . . . . . . . . . . . . . . . . 8065752188
Active FMS Pack, 0.9 mm Mini-Flared ABS® 45° Kelman® . . . . . . . . . . . . . . . . 8065752189
Active FMS Pack, 0.9 mm Mini-Flared ABS® 30° OZil®. . . . . . . . . . . . . . . . . . 8065752190
Active FMS Pack, 0.9 mm Mini-Flared ABS® 45° OZil®. . . . . . . . . . . . . . . . . . 8065752191
Active FMS Pack, 0.9 mm INTREPID® Ultra, Mini-Flared ABS® 30° Kelman®. . . . . . 8065752192
Active FMS Pack, 0.9 mm INTREPID® Ultra, Mini-Flared ABS® 45° Kelman®. . . . . . 8065752193
Active FMS Pack, 0.9 mm INTREPID® Ultra, Mini-Flared ABS® 30° OZil® . . . . . . . 8065752194
Active FMS Pack, 0.9 mm INTREPID® Ultra, Mini-Flared ABS® 45° OZil® . . . . . . . 8065752195
Active FMS Pack, 0.9 mm INTREPID® Nano, Mini-Flared ABS® 30° Kelman® . . . . . 8065752196
Active FMS Pack, 0.9 mm INTREPID® Nano, Mini-Flared ABS® 45° Kelman® . . . . . 8065752197
Active FMS Pack, 0.9 mm INTREPID® Nano, Mini-Flared ABS® 30° OZil®. . . . . . . 8065752198
Active FMS Pack, 0.9 mm INTREPID® Nano, Mini-Flared ABS® 45° OZil®. . . . . . . 8065752199
Active FMS Pack, 0.9 mm INTREPID® Ultra, ABS® INTREPID® Balanced 30°. . . . . 8065752200
Active FMS Pack, 0.9 mm INTREPID® Ultra, ABS® INTREPID® Balanced 45°. . . . . 8065752201
Active FMS Pack, 0.9 mm INTREPID® Nano, ABS® INTREPID® Balanced 30° . . . . . 8065752202
Active FMS Pack, 0.9 mm INTREPID® Nano, ABS® INTREPID® Balanced 45° . . . . . 8065752203
Active FMS Pack, 0.9 mm INTREPID® Ultra, ABS® Mini 30° Kelman® . . . . . . . . . 8065752244
Active FMS Pack, 0.9 mm INTREPID® Ultra, ABS® Mini 45° Kelman® . . . . . . . . . 8065752245
Active FMS Pack, 0.9 mm INTREPID® Nano, ABS® Mini 30° Kelman® . . . . . . . . . 8065752246
Active FMS Pack, 0.9 mm INTREPID® Nano, ABS® Mini 45° Kelman® . . . . . . . . . 8065752247
6.2
FOR REFERENCE ONLY 8065751772
 DESCRIPTION CATALOG NUMBER

CENTURION® FMS Packs for Active Fluidics™ Technology, 0.7 mm

Active FMS Pack, Basic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752180
Active FMS Pack, 0.7 mm INTREPID® Ultra Tipless . . . . . . . . . . . . . . . . . . . 8065752479
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® Mini 30° Kelman® . . . . . . . . . 8065752480
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® Mini 45° Kelman® . . . . . . . . . 8065752481
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® Mini 30° OZil®. . . . . . . . . . . 8065752482
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® Mini 45° OZil®. . . . . . . . . . . 8065752483
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® Mini 30° Reverse OZil®. . . . . . . 8065752484
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® INTREPID® Balanced 30°. . . . . 8065752485
Active FMS Pack, 0.7 mm INTREPID® Ultra, ABS® INTREPID® Balanced 45°. . . . . 8065752486
Active FMS Pack, 0.7 mm INTREPID® Nano Tipless. . . . . . . . . . . . . . . . . . . 8065752487
Active FMS Pack, 0.7 mm INTREPID® Nano, 30° Kelman® ABS® Mini . . . . . . . . . 8065752488
Active FMS Pack, 0.7 mm INTREPID® Nano, 45° Kelman® ABS® Mini . . . . . . . . . 8065752489
Active FMS Pack, 0.7 mm INTREPID® Nano, 30° OZil® ABS® Mini . . . . . . . . . . . 8065752490
Active FMS Pack, 0.7 mm INTREPID® Nano, 45° OZil® ABS® Mini . . . . . . . . . . . 8065752491
Active FMS Pack, 0.7 mm INTREPID® Nano, 30° Reverse OZil® ABS® Mini . . . . . . 8065752492
Active FMS Pack, 0.7 mm INTREPID® Nano, ABS® INTREPID® Balanced 30° . . . . . 8065752493
Active FMS Pack, 0.7 mm INTREPID® Nano, ABS® INTREPID® Balanced 45° . . . . . 8065752494

CENTURION® FMS Packs for Gravity Fluidics

Gravity FMS Pack, Basic. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752212
Gravity FMS Pack, 0.9 mm Tipless. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752213
Gravity FMS Pack, 0.9 mm INTREPID® Ultra Tipless. . . . . . . . . . . . . . . . . . . 8065752214
Gravity FMS Pack, 0.9 mm INTREPID® Nano Tipless . . . . . . . . . . . . . . . . . . 8065752215
Gravity FMS Pack, 0.9 mm INTREPID® Ultra, ABS® INTREPID® Balanced 30°. . . . . 8065752216
Gravity FMS Pack, 0.9 mm INTREPID® Ultra, ABS® INTREPID® Balanced 45° . . . . 8065752217

BSS® Irrigating Solution

(Catalog numbers provided for U.S. customers. International customers should contact their local
distributor for order information.)
BSS® Sterile Irrigating Solution, 500 ml Bag. . . . . . . . . . . . . . . . . . . . . . . . 0007950185
BSS® Sterile Irrigating Solution, 500 ml Bottle. . . . . . . . . . . . . . . . . . . . . . . 0065079550
BSS® Sterile Irrigating Solution, 250 ml Bottle. . . . . . . . . . . . . . . . . . . . . . . 0065079525
BSS PLUS® Sterile Intraocular Irrigating Solution, 500 ml Bottle . . . . . . . . . . . . . 0065080050
BSS PLUS® Sterile Intraocular Irrigating Solution, 250 ml Bottle . . . . . . . . . . . . . 0065080025
BSS PLUS® Sterile Intraocular Irrigating Solution, 500 ml Bag . . . . . . . . . . . . . . 0008000086

Phaco Tips
ALCON® UltraChopper® Tip. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751789
30° Round, 0.9 mm ABS ®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065790020
45° Round, 0.9 mm ABS ®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065790021
30° Kelman®, 0.9 mm ABS ® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065790022
45° Kelman®, 0.9 mm ABS ® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065790023
30° Round, 0.9 mm MicroTip Flared ABS®. . . . . . . . . . . . . . . . . . . . . . . . . 8065740837
8065751772 6.3
FOR REFERENCE ONLY
 DESCRIPTION CATALOG NUMBER

45° Round, 0.9 mm MicroTip Flared ABS®. . . . . . . . . . . . . . . . . . . . . . . . . 8065740838

30° Kelman®, 0.9 mm MicroTip Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . 8065740839
45° Kelman®, 0.9 mm MicroTip Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . 8065740840
30° Round, 0.9 mm Tapered ABS®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750261
45° Round, 0.9 mm Tapered ABS®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750262
30° Kelman®, 0.9 mm Tapered ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750263
45° Kelman®, 0.9 mm Tapered ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750264
30° Kelman®, 0.9 mm Mini Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750852
45° Kelman®, 0.9 mm Mini Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . 8065750853
30° OZil® 12, 0.9 mm Mini Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751176
45° OZil® 12, 0.9 mm Mini Flared ABS® . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751177
30° Reverse OZil® 12, 0.9 mm Mini Flared ABS® . . . . . . . . . . . . . . . . . . . . . 8065751178
30° Kelman®, 0.9 mm Mini ABS®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752065
45° Kelman®, 0.9 mm Mini ABS®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065752066

Irrigation/Aspiration Accessories
INTREPID® Bimanual Polymer I/A Set . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751922
INTREPID® Coaxial Polymer I/A Handpiece – Flared Tip, Straight. . . . . . . . . . . . 8065751919
INTREPID® Coaxial Polymer I/A Handpiece – Flared Tip, Angled . . . . . . . . . . . . 8065751920
INTREPID® Coaxial Polymer I/A Handpiece – Flared Tip, Curved . . . . . . . . . . . . 8065751921
INTREPID® Coaxial Polymer I/A Handpiece – Tapered Tip, Straight. . . . . . . . . . . 8065752144
INTREPID® Coaxial Polymer I/A Handpiece – Tapered Tip, Angled. . . . . . . . . . . 8065752145
INTREPID® Coaxial Polymer I/A Handpiece – Tapered Tip, Curved . . . . . . . . . . . 8065752146
INTREPID® Polymer I/A Tip, Straight. . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751510
INTREPID® Polymer I/A Tip, Angled . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751511
INTREPID® Polymer I/A Tip, Curved. . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751512
I/A Tip 0.3 mm Small Bore. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 356-1007
I/A Tip 0.3 mm Bent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 356-1010
Ultraflow™* II Handpiece. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751795
Ultraflow™* Tip Protector, Standalone. . . . . . . . . . . . . . . . . . . . . . . . . . . 8065817002
I/A Tip .033 OD, .3 mm, INTREPID® . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065751012
I/A Tip .033 OD, .3 mm Bent, INTREPID®. . . . . . . . . . . . . . . . . . . . . . . . .8065751013
Silicone I/A Tip, Bent. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065740969
Silicone I/A Tip, Straight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065740970

6.4
FOR REFERENCE ONLY 8065751772
Bipolar Accessories
Brush (20 Ga). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065804201
Brush (18 Ga). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065804001
Brush (23 Ga). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065807901
Straight Iris Forceps Without Cable. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065129501
Coaptation Forceps Without Cable. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065129301
Curved Iris Bipolar Forceps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065129101
4" Straight Forceps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065127501
3-1/2" Curved Iris. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065128001
4-1/4" Coaptation, Extra Fine. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8065128201
Kirwan Surgical Products (cables)
12 ft (3.6m) Silicone (Reuse). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6000V
12 ft (3.6m) Thermoplastic Rubber (Reuse) . . . . . . . . . . . . . . . . . . . . . . . . 10-5000V
28.6 mm Disposable Bipolar Cable, 12ft (3.6m, SU). . . . . . . . . . . . . . . . . . . . 10-4000V
28.6 mm Disposable Bipolar Cable, 12ft (3.6m, SU). . . . . . . . . . . . . . . . . . . . 10-4001V
Braun (cables)
Aesculap. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .GK291 SU
Aesculap. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .GK331

Anterior Vitrectomy
23 Ga CENTURION® UltraVit® Anterior Vitrectomy Probe. . . . . . . . . . . . . . . . 8065752134

8065751772 6.5
FOR REFERENCE ONLY
 THIS PAGE INTENTIONALLY BLANK

6.6
FORLAST
REFERENCE
PAGE OF THIS SECTION
ONLY 8065751772
 SECTION SEVEN
INDEX

Symbols C

23 gauge Centurion® UltraVit® probe. . . . . . . . . . . . . 2.26 Cannula . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.26

Capsulorhexis. . . . . . . . . . . . . . . . . . . . . . . . . 2.27
A Capsulotomy . . . . . . . . . . . . . . . . . . . . . . . . . 2.63
Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . 1.24 Capsulotomy device. . . . . . . . . . . . . . . . . . . . . . 2.27
About dialog. . . . . . . . . . . . . . . . . . . . . . . . . . 2.60 Capsulotomy step. . . . . . . . . . . . . . . . . . . . 2.12, 3.17
ABS® phaco tip. . . . . . . . . . . . . . . . . . . . . . . . .2.21 Care and maintenance. . . . . . . . . . . . . . . . . . . . . .4.1
Accessories . . . . . . . . . . . . . . . . . . . . . . . . 6.1, 6.2 Care of the Centurion® Vision System. . . . . . . . . . . . . 4.4
Accessory drawer. . . . . . . . . . . . . . . . . . . . . . . .2.4 Cartridge selection button. . . . . . . . . . . . . . . . . . . 2.85
Accessory equipment . . . . . . . . . . . . . . . . . . . . . .1.3 Cartridge type button . . . . . . . . . . . . . . . . . . . . . 3.10
AC power cord hanger . . . . . . . . . . . . . . . . . . . . . 2.5 Caster wheels . . . . . . . . . . . . . . . . . . . . . . . . . .2.5
AC power switch. . . . . . . . . . . . . . . . . . . . . . . . 2.5 Cautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . xii
AcrySof® intraocular lenses . . . . . . . . . . . . . . . . . . 2.24 CDE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.43
Active Fluidics™ system . . . . . . . . . . . . . . . . .2.7, 2.68 Centurion® fluidic management system packs. . . . . . . . 2.30
Active Fluidics™ bag bay. . . . . . . . . . . . . . . . . 2.6, 2.7 Centurion® FMS pack setup procedure. . . . . . . . . . . . .3.3
Active Fluidics™ technology. . . . . . . . . . . . . . . . . 2.69 Centurion® footswitch. . . . . . . . . . . . . . . . . . . . . .2.8
Advisories. . . . . . . . . . . . . . . . . . . . . . . . .5.1, 5.10 Centurion® OZil® handpiece . . . . . . . . . . . . . . . . . 2.19
Alcon default settings. . . . . . . . . . . . . . . . . . . . . 1.29 Centurion® UltraVit® anterior vitrectomy probe. . . . . . . . 6.5
Alcon Laboratories. . . . . . . . . . . . . . . . . . . . . . . . i Centurion® UltraVit® probe. . . . . . . . . . . . . . . . . . 2.26
Alcon Laboratories (UK) Ltd.. . . . . . . . . . . . . . . . . . . i Centurion® UltraVit® probe setup. . . . . . . . . . . . 3.13, 3.16
Alcon Research . . . . . . . . . . . . . . . . . . . . . . . . . . i Centurion® Vision System . . . . . . . . . . . . . . . . . . . 1.1
Alcon Sales Department . . . . . . . . . . . . . . . . . . . . 6.1 Centurion® vitrectomy cutter . . . . . . . . . . . . . . . . . 2.89
Alcon settings. . . . . . . . . . . . . . . . . . . . . . 2.37, 2.77 Change remote channel dialog. . . . . . . . . . . . . . . . 2.18
Alcon Technical Services Department. . . . . . . . . . xii, 1.22 Charging footswitch battery. . . . . . . . . . . . . . . . . . 2.13
Logicware. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60 Charging station. . . . . . . . . . . . . . . . . . . . . . . . .2.5
Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xii Check‑out procedure. . . . . . . . . . . . . . . . . . . . . . 3.1
Vent test. . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.3 Check-out tests. . . . . . . . . . . . . . . . . . . . . . . . 1.17
Antenna . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.5 Clean footswitch . . . . . . . . . . . . . . . . . . . . . . . . 4.3
Anterior vitrectomy (Anterior Vit). . . . . . . . . . . 2.90, 3.13 Clean handpieces . . . . . . . . . . . . . . . . . . . . . . . .4.2
Anterior vitrectomy mode of operation. . . . . . . . . . . . 2.89 Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . .4.4
Anterior vitrectomy probe. . . . . . . . . . . . . . . . . . . .6.5 Clean the footswitch . . . . . . . . . . . . . . . . . . . . . 1.17
Ant Vit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.89 CME compliant video overlay . . . . . . . . . . . . . . . . 2.51
Ant Vit step . . . . . . . . . . . . . . . . . . . . . . . 3.13, 3.16 Coagulation . . . . . . . . . . . . . . . . . . . . . . . . . . 1.19
Aspiration Bypass System (ABS). . . . . . . . . . . . . . . 2.21 Coagulation sccessories. . . . . . . . . . . . . . . . . . . . 2.27
Aspiration control. . . . . . . . . . . . . . . . . . . . . . . 2.83 Coagulation handpiece setup . . . . . . . . . . . . . . . . . 3.17
Aspiration settings . . . . . . . . . . . . . . . . . . . . . . 2.71 Coagulation mode of operation. . . . . . . . . . . . . . . . 2.87
Aspiration/Vacuum adjustments . . . . . . . . . . . . . . . 1.16 Coagulation power . . . . . . . . . . . . . . . . . . . . . . 1.28
Audio input . . . . . . . . . . . . . . . . . . . . . . . . . . .2.5 Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3
Audio speakers. . . . . . . . . . . . . . . . . . . . . . . . . 2.4 Connect phaco handpiece. . . . . . . . . . . . . . . . . . . .3.6
AutoSert® IOL Injector Setup. . . . . . . . . . . . . . 2.73, 3.10 Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.2
AutoSert® full extension offset. . . . . . . . . . . . . . . . 2.51 Constellation® footswitch. . . . . . . . . . . . . . . . . . . .2.8
AutoSert® IOL Injector. . . . . . . . . . . . . . 2.24, 2.84, 3.10 Consumable items. . . . . . . . . . . . . . . . . . . . . . . 2.29
AutoSert® mode of operation . . . . . . . . . . . . . . . . . 2.84 Consumable pack configurations . . . . . . . . . . . . . . . 2.29
AutoSert® remote default. . . . . . . . . . . . . . . . . . . 2.51 Consumable packs . . . . . . . . . . . . . . . . . . . . . . 1.21
AutoSert® injector step . . . . . . . . . . . . . . 2.74, 2.82, 3.10 Contact information. . . . . . . . . . . . . . . . . . . . . . .5.1
Continuous irrigation . . . . . . . . . . . . . . . 2.12, 2.48, 2.71
B Continuous irrigation auto-off threshold. . . . . . . . . . . 2.48
Continuous phaco mode. . . . . . . . . . . . . . . . . . . . 2.79
Backup doctor. . . . . . . . . . . . . . . . . . . . . . . . . 2.56 Copy doctor. . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Bag bay for Active Fluidics™ technology. . . . . . 2.6, 3.3, 2.7 Copy procedure. . . . . . . . . . . . . . . . . . . . . . . . 2.40
Battery status. . . . . . . . . . . . . . . . . . . . . . . . . 2.43 Corrective action. . . . . . . . . . . . . . . . . . . . . . . . 5.5
Bipolar coagulation accessories. . . . . . . . . . . . . .2.27, 6.5 Cumulative Dissipated Energy (CDE). . . . . . . . . . . . 2.43
Bottle height. . . . . . . . . . . . . . . . . . . . . . . . . . 2.71 Custom / About . . . . . . . . . . . . . . . . . . . . . . . . 2.60
BSS® irrigating fluid. . . . . . . . . . . . 2.6, 2.7, 2.28, 2.30, 6.3 Custom / Backup/Restore / Backup Tab . . . . . . . . . . . 2.56
Burst Phaco mode. . . . . . . . . . . . . . . . . . . . . . . 2.81 Custom / Backup/Restore / Restore Tab . . . . . . . . . . . 2.56
Button assignment. . . . . . . . . . . . . . . . . . . . 2.11, 2.49 Custom button. . . . . . . . . . . . . . . . . . . . . . 2.46, 2.66
Custom / Doctor Settings / Advanced Tab . . . . . . . . . . 2.51
Custom / Doctor Settings / Fluidics Tab . . . . . . . . . . . 2.48

8065751772 7.1
FOR REFERENCE ONLY
Custom / Doctor Settings / Footswitch Tab. . . . . . . . . . 2.49 Fill button. . . . . . . . . . . . . . . . . . . . . . . . 2.62, 3.13
Custom / Doctor Settings / General Tab . . . . . . . . . . . 2.47 Fill step. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.4
Custom / Doctor Settings / SGS Tab. . . . . . . . . . . . . 2.50 Fill step for Irrigation/Aspiration. . . . . . . . . . . . . . . 2.83
Custom / Doctor Settings / Sounds Tab. . . . . . . . . . . . 2.50 Fill test chamber. . . . . . . . . . . . . . . . . . . . . . . . .3.7
Custom Pak™* . . . . . . . . . . . . . . . . . . . . . . . . 2.29 Final Rate (mm/s). . . . . . . . . . . . . . . . . . . . 2.86, 3.11
Custom / Procedure Builder. . . . . . . . . . . . . . . . . . 2.57 Fixed aspiration control. . . . . . . . . . . . . . . . . . . . 2.83
Custom / Save. . . . . . . . . . . . . . . . . . . . . . . . . 2.52 Fixed coagulation control. . . . . . . . . . . . . . . . . . . 2.87
Custom / Save As . . . . . . . . . . . . . . . . . . . . . . . 2.52 Fixed footpedal control . . . . . . . . . . . . . . . . . .2.9, 2.78
Custom / Shutdown. . . . . . . . . . . . . . . . . . . . . . .4.2 Fixed vacuum control. . . . . . . . . . . . . . . . . . . . . 2.83
Custom / Shutdown System. . . . . . . . . . . . . . . . . . 2.61 Flash drive. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Custom / System Settings / General Tab. . . . . . . . . . . 2.53 Fluidic Management System (FMS). . . . . . . . 2.28, 2.30, 3.3
Custom / System Settings / Wireless Tab. . . . . . . . . . . 2.55 Fluidics administration. . . . . . . . . . . . . . . . . . 2.7, 2.68
Custom / View Events. . . . . . . . . . . . . . . . . . . . . 2.60 Fluidics bags . . . . . . . . . . . . . . . . . . . . . . . . . . 4.8
Fluidics controls. . . . . . . . . . . . . . . . . . . . . 2.64, 2.68
D Fluidics control window . . . . . . . . . . . . . . . . . . . 2.69
Date and time . . . . . . . . . . . . . . . . . . . . . . . . . 2.53 Fluidics module. . . . . . . . . . . . . . . . . . . 2.2, 2.3, 2.28
D/C cartridge. . . . . . . . . . . . . . . . . . . . . . 2.24, 3.10 FMS. . . . . . . . . . . . . . . . . . . . . . . . .2.28, 2.30, 3.3
Default PEL. . . . . . . . . . . . . . . . . . . . . . . . . . 2.47 FMS packs . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.2
Default procedure. . . . . . . . . . . . . . . . . . . . . . . 2.47 FMS pack setup procedure. . . . . . . . . . . . . . . . . . . 3.3
Default settings . . . . . . . . . . . . . . . . . . . . . . . . 1.29 Footpedal control . . . . . . . . . . . . . . . . . . . . . . . .2.9
Delete doctor. . . . . . . . . . . . . . . . . . . . . . . . . 2.38 Footpedal detents . . . . . . . . . . . . . . . . . . . . . . . 2.11
Delete procedure . . . . . . . . . . . . . . . . . . . . . . . 2.40 Footpedal positions . . . . . . . . . . . . . . . . . . . . . . .2.9
Description of Centurion® Vision System . . . . . . . . . . . 2.1 Footpedal spans. . . . . . . . . . . . . . . . . . . . . . . . 2.11
Description of console . . . . . . . . . . . . . . . . . . . . . 2.2 Footpedal vibration . . . . . . . . . . . . . . . . . . . 2.11, 2.49
Description of footswitch. . . . . . . . . . . . . . . . . . . .2.8 Footswitch. . . . . . . . . . . . . . . . . . . . . . . . .1.17, 2.8
Description of IR remote control . . . . . . . . . . . . . . . 2.15 Footswitch battery. . . . . . . . . . . . . . . . . . . . . . . 2.13
Detents . . . . . . . . . . . . . . . . . . . . . . . . . 2.11, 2.49 Footswitch battery status. . . . . . . . . . . . . . . . . . . 2.43
DFU. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.29, 2.30 Footswitch button. . . . . . . . . . . . . . . . . . . . . . . 2.43
Dialogs . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.35 Footswitch button assignments . . . . . . . . . . . . . . . . 2.11
Directions for use. . . . . . . . . . . . . . . . . . . . 2.29, 2.30 Footswitch cable . . . . . . . . . . . . . . . . . . . . . . . 2.14
Disable the vit cutter . . . . . . . . . . . . . . . . . . . . . 2.89 Footswitch channel . . . . . . . . . . . . . . . . . . . . . . 2.55
Display panel . . . . . . . . . . . . . . . . . . . . . . .2.3, 2.35 Footswitch cleaning. . . . . . . . . . . . . . . . . . . . . . .4.3
Display screens . . . . . . . . . . . . . . . . . . . . . . . . 2.35 Footswitch connectors . . . . . . . . . . . . . . . . . . . . 2.14
Doctor Name button. . . . . . . . . . . . . . . . . . . . . . 2.37 Footswitch floor security. . . . . . . . . . . . . . . . . . . 2.14
Doctor Name dialog. . . . . . . . . . . . . . . . . . . . . . 2.52 Footswitch hanger / charging station . . . . . . . . . . . . . .2.5
Doctor settings . . . . . . . . . . . . . . . . . . . . . . . . 2.46 Footswitch icon button. . . . . . . . . . . . . . . . . . . . . 2.8
Doctor Settings dialog. . . . . . . . . . . . . . . . . . . . . 2.47 Footswitch network. . . . . . . . . . . . . . . . . . . . . . 2.55
Doctor Settings dialog screen. . . . . . . . . . . . . . . . . 2.10 Footswitch network region . . . . . . . . . . . . . . . . . . 2.55
D or C cartridge. . . . . . . . . . . . . . . . . . . . . . . . 2.85 Footswitch range spans . . . . . . . . . . . . . . . . . . . . 2.49
Drawer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.4 Footswitch signal strength . . . . . . . . . . . . . . . . . . 2.43
Drop list menu items. . . . . . . . . . . . . . . . . . . . . 2.46 Footswitch status. . . . . . . . . . . . . . . . . . . . . . . 2.13
Front connector panel. . . . . . . . . . . . . . . . . . . . . 2.42
E Front display panel and touch screen. . . . . . . . . . . . . 2.35
Front panel button. . . . . . . . . . . . . . . . . . . . . . . 2.42
Edit procedure comments. . . . . . . . . . . . . . . . . . . 2.40 Front panel connectors. . . . . . . . . . . . . . . . . . . . . 2.3
EMC statements. . . . . . . . . . . . . . . . . . . . . . . . .1.4 Fuse door. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.5
Enable. . . . . . . . . . . . . . . . . . . . . . . . . . 2.12, 3.17 Fuse replacement . . . . . . . . . . . . . . . . . . . . . . . .4.6
Enable and disable the Vit cutter. . . . . . . . . . . . . . . 2.89
Enter key . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.17 G
Environmental considerations. . . . . . . . . . . . . . . . . .1.4
Epinucleus removal (Epi removal) . . . . . . . . . . . . . . 2.90 Gravity fluidics. . . . . . . . . . . . . . . . . . . 2.7, 2.68, 2.69
Eq. bottle height. . . . . . . . . . . . . . . . . . . . . . . . 2.71 Gravity fluidics FMS. . . . . . . . . . . . . . . . . . . . . 2.68
Equipotential ground connector. . . . . . . . . . . . . . . . .2.5 Ground connector. . . . . . . . . . . . . . . . . . . . . . . .2.5
Estimated leakage comp . . . . . . . . . . . . . . . . . . . 2.48 Guidance and manufacturer's declaration. . . . . . . . . .1.5,1.6
Ethernet internet communications (RS422). . . . . . . . . . .2.5 H
Event . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60, 5.1
Event codes . . . . . . . . . . . . . . . . . . . . . . . . . . 5.10 Handle bar. . . . . . . . . . . . . . . . . . . . . . . . . . . .2.5
Event message. . . . . . . . . . . . . . . . . . . . . . . . . .4.1 Handpiece connectors. . . . . . . . . . . . . . . . . . .2.3, 2.42
Handpieces. . . . . . . . . . . . . . . . . . . . . . . . . . 2.19
F Handpiece tips. . . . . . . . . . . . . . . . . . . . . . . . . .3.5
Faults. . . . . . . . . . . . . . . . . . . . . . . . . 5.1, 5.3, 5.10 Hardware. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
FAX. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . i Hazardous substances. . . . . . . . . . . . . . . . . . . . . 1.10
Federal Communications Commission (FCC). . . . . . . . . 1.8
Field service engineers. . . . . . . . . . . . . . . . . . . . . 4.1

7.2
FOR REFERENCE ONLY 8065751772
I Linear aspiration control . . . . . . . . . . . . . . . . . . . 2.83
Linear coagulation control . . . . . . . . . . . . . . . . . . 2.87
I/A cut. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.91 Linear footpedal control. . . . . . . . . . . . . . . . . .2.9, 2.78
I/A handpiece . . . . . . . . . . . . 1.15, 2.23, 2.82, 3.2, 3.9, 6.4 Linear vacuum control . . . . . . . . . . . . . . . . . . . . 2.83
I/A tip . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6.4 List of figures . . . . . . . . . . . . . . . . . . . . . . . . . viii
I/A tip wrench. . . . . . . . . . . . . . . . . . . . . . . . . 2.30 List of tables. . . . . . . . . . . . . . . . . . . . . . . . . . . xi
ICD. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.27, 2.63 Load a plunger . . . . . . . . . . . . . . . . . . . . . . . . 3.11
Icons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.25 Load plunger button. . . . . . . . . . . . . . . . . . . 2.85, 3.11
Import procedure from doctor. . . . . . . . . . . . . . . . . 2.40 Locking caster wheels. . . . . . . . . . . . . . . . . . . . . .2.5
Indications for use. . . . . . . . . . . . . . . . . . . . . . . .1.3 Longitudinal power. . . . . . . . . . . . . . . . . . . . . . 2.78
Industry of Canada (IC). . . . . . . . . . . . . . . . . . . . .1.9 Longitudinal pulse duration. . . . . . . . . . . . . . . . . . 2.67
INFINITI® OZil® handpiece. . . . . . . . . . . . . . . . . . 2.19 Longitudinal / Torsional ratio. . . . . . . . . . . . . . . . . 2.67
Infusion sleeves. . . . . . . . . . . . . 2.30, 2.19, 2.22, 3.5, 3.9
Initial rate (mm/s). . . . . . . . . . . . . . . . . . . . 2.86, 3.11 M
Initial system setup . . . . . . . . . . . . . . . . . . . . . . .3.2
Injector . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.24 Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . .4.1
Input/Output (I/O) connector panel. . . . . . . . . . . . . . .2.5 Maintenance schedules . . . . . . . . . . . . . . . . . . . . .4.4
Instrument tray . . . . . . . . . . . . . . . . . . . . . . . . . 2.3 Malfunctioning parts or components . . . . . . . . . . . . . .5.1
Intelligent Phaco (IP) . . . . . . . . . . . . . . . . . . . . . 2.67 Manage doctors. . . . . . . . . . . . . . . . . . . . . 2.37, 2.38
Intraocular lenses . . . . . . . . . . . . . . . . . . . . . . . 2.24 Manage doctors dialog. . . . . . . . . . . . . . . . . . . . 2.38
Intraocular pressure (IOP). . . . . . . . . . . . . . . . .2.7, 2.68 Manage procedures dialog . . . . . . . . . . . . . . . . . . 2.40
INTREPID® AutoSert® IOL injector . . . . . . . 2.24, 2.84, 3.10 Manage procedures dialog . . . . . . . . . . . . . . . . . . 2.41
INTREPID® AutoSert® IOL injector setup. . . . . . . . . . 3.10 Manual revision record . . . . . . . . . . . . . . . . . . . . . ii
INTREPID® capsulotomy device. . . . . . . . . . . . . . . 2.63 Metal plunger . . . . . . . . . . . . . . . . . . . . . . . . . 3.11
INTREPID® capsulotomy device. . . . . . . . . . . . . . . 3.17 Metrics dialog. . . . . . . . . . . . . . . . . . . . . . . . . 2.43
INTREPID® capsulotomy device setup. . . . . . . . . . . . 3.17 MicroSmooth® infusion sleeves. . . . . . . . . . . . . . . . 2.22
INTREPID® cartridge. . . . . . . . . . . . . . . 2.24, 2.85, 3.10 Mode button. . . . . . . . . . . . . . . . . . . . . . . . . . 2.65
INTREPID® Nano infusion sleeves . . . . . . . . . . . . . 2.22 Modify system settings . . . . . . . . . . . . . . . . . . . . 2.46
INTREPID® Ultra infusion sleeves . . . . . . . . . . . . . 2.22 N
IOL cartridge. . . . . . . . . . . . . . . . . . . . . . . . . 3.11
IOL injector. . . . . . . . . . . . . . . . . 1.16, 2.24, 2.84, 3.10 Nano infusion sleeves. . . . . . . . . . . . . . . . . . . . . 2.22
IOP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.7 New doctor. . . . . . . . . . . . . . . . . . . . . . . . . . 2.38
IOP control. . . . . . . . . . . . . . . . . . . . . . . . . . 2.68 New step. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.57
IOP ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.72 Next button. . . . . . . . . . . . . . . . . . . . . . . . . . 3.13
IOP setpoints . . . . . . . . . . . . . . . . . . . . . . . . . 2.70
IP button. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.67 O
IP settings dialog. . . . . . . . . . . . . . . . . . . . . . . 2.67 Observations/symptoms. . . . . . . . . . . . . . . . . . . . .5.1
Irr/Asp mode . . . . . . . . . . . . . . . . . . . . . . . . . 2.82 Observed conditions. . . . . . . . . . . . . . . . . . . . . . .5.5
IR remote control . . . . . . . . . . . . . . . . . . . . . . . 2.15 Occlusion tones. . . . . . . . . . . . . . . . . . . . . . . . 1.18
Irr factor. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.72 Operating instructions. . . . . . . . . . . . . . . . . . . . . .3.1
Irrigating cannula . . . . . . . . . . . . . . . . . . . . 2.26, 3.14 Operating parameter settings . . . . . . . . . . . . . . . . . 2.65
Irrigating fluid. . . . . . . . . . . . . . . . . 2.6, 2.7, 2.28, 2.30 Oval display buttons . . . . . . . . . . . . . . . . . . . . . 2.66
Irrigating solution. . . . . . . . . . . . . . . . . . . . . . . .6.3
Irrigation/Aspiration accessories . . . . . . . . . . . . . . . .6.4 P
Irrigation/Aspiration Cut (I/A Cut) . . . . . . . . . . . . . . 2.91
Irrigation/Aspiration handpiece setup. . . . . . . . . . . . . .3.9 Packing system for transit. . . . . . . . . . . . . . . . . . . .4.7
Irrigation/Aspiration mode of operation . . . . . . . . . . . 2.82 Packs . . . . . . . . . . . . . . . . . . . . . . . . 1.21, 2.30, 6.2
Irrigation fill. . . . . . . . . . . . . . . . . . . . . . . . . . 2.53 Pairing footswitch with Centurion® system. . . . . . . . . . 2.13
Irrigation pressure. . . . . . . . . . . . . . . . . . . . . . . 2.12 Pairing of the footswitch. . . . . . . . . . . . . . . . . . . . 2.8
Irrigation pressure drop. . . . . . . . . . . . . . . . . . . . 2.49 Pairing of the SGS device. . . . . . . . . . . . . . . . . . . 2.13
Irrigation tone. . . . . . . . . . . . . . . . . . . . . . . . . 2.51 Pairing of the surgical guidance system. . . . . . . . . . . . 2.54
Irrigation type default. . . . . . . . . . . . . . . . . . . . . 2.53 Parameter selection button. . . . . . . . . . . . . . . . . . 2.15
IV pole. . . . . . . . . . . . . . . . . . . . . .1.17, 2.7, 3.3, 3.4 Parameter settings. . . . . . . . . . . . . . . . . . . . 2.65, 2.66
IV pole settings . . . . . . . . . . . . . . . . . . . . . . . . 2.68 Parameter value adjustment keys. . . . . . . . . . . . . . . 2.17
Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6.1
K Patents. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Patient Eye Level (PEL) . . . . . . . . . . . . . . . . . 2.47, 3.8
Key features of the Centurion® Vision System. . . . . . . . .1.2 Pause . . . . . . . . . . . . . . . . . . . . . . . . . . 2.86, 3.11
L PEL. . . . . . . . . . . . . . . . . . . . . . . . . 2.47, 2.71, 3.8
PEL button . . . . . . . . . . . . . . . . . . . . . . . . . . 2.63
Labels used on the Centurion® Vision System. . . . . . . . 1.26 PEL verification. . . . . . . . . . . . . . . . . . . . . . . . .3.8
Language. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.53 Performance requirements . . . . . . . . . . . . . . . . . . 1.24
Lens insertion. . . . . . . . . . . . . . . . . . . . . . . . . 2.85 Peripheral iridotomy (Peripheral Irid) . . . . . . . . . . . . 2.91
Light button. . . . . . . . . . . . . . . . . . . . . . . . . . 2.66 Phaco handpiece care. . . . . . . . . . . . . . . . . . . . . 1.13
Limited warranty. . . . . . . . . . . . . . . . . . . . . . . 1.23 Phaco handpiece connectors . . . . . . . . . . . . . . . . . . 2.3

8065751772 7.3
FOR REFERENCE ONLY
Phaco handpieces . . . . . . . . . . . . . . . . . . . . . . . 2.19 S
Phaco handpiece setup and test. . . . . . . . . . . . . . . . .3.5
Phaco handpiece tip/infusion sleeve preparation. . . . . . . .3.6 Safety performance . . . . . . . . . . . . . . . . . . . . . . 1.22
Phaco handpiece tips. . . . . . . . . . . . . . . . . . . . . 1.14 Sales department . . . . . . . . . . . . . . . . . . . . . . . . 6.1
Phaco handpiece tips and corresponding infusion sleeves . . . 3.5 Save dialog. . . . . . . . . . . . . . . . . . . . . . . . . . 2.52
Phaco mode of operation . . . . . . . . . . . . . . . . . . . 2.78 Secure the display screen and instrument tray. . . . . . . . . 4.7
Phaco timing configurations . . . . . . . . . . . . . . . . . 2.79 Select a cartridge. . . . . . . . . . . . . . . . . . . . . . . 3.10
Phaco tips . . . . . . . . . . . . . . . . . . . . . . . . . . . .6.3 Select Doctor dialog. . . . . . . . . . . . . . . . . . . . . . 2.62
Phone number. . . . . . . . . . . . . . . . . . . . . . . . . 2.60 Self-test . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.1
Power/Amplitude . . . . . . . . . . . . . . . . . . . . . . . 2.78 Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.22
Power/Amplitude dialogs. . . . . . . . . . . . . . . . . . . 2.78 Setting Patient Eye Level (PEL) . . . . . . . . . . . . . . . . 3.8
Power cord hanger . . . . . . . . . . . . . . . . . . . . . . . 2.5 Setup and check‑out. . . . . . . . . . . . . . . . . . . . . . .3.1
Power IV pole. . . . . . . . . . . . . . . . . . . . . . . . . .2.7 Setup button. . . . . . . . . . . . . . . . . . . . . . . . . . 2.77
Power module fuse door . . . . . . . . . . . . . . . . . . . . 4.6 Setup screen. . . . . . . . . . . . . . . . . . . . . . . 2.35, 2.36
Power switch. . . . . . . . . . . . . . . . . . . 2.4, 2.5, 3.1, 4.2 Setup status window . . . . . . . . . . . . . . . . . . . . . 2.45
Power up sequence. . . . . . . . . . . . . . . . . . . . . . . 3.1 Setup steps . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62
Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . xii SGS . . . . . . . . . . . . . . . . . . . . . . . . 2.43, 2.50, 2.54
Preface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xii SGS pairing. . . . . . . . . . . . . . . . . . . . . . . . . . 2.54
Preload an IOL. . . . . . . . . . . . . . . . . . . . . . . . 3.11 SGS pairing indicator. . . . . . . . . . . . . . . . . . . . . 2.43
Preload IOL button. . . . . . . . . . . . . . . . . . . 2.85, 3.11 Shut down sequence. . . . . . . . . . . . . . . . . . . . . . .3.1
Preparing test chamber. . . . . . . . . . . . . . . . . . . . . 3.6 Shut down the system. . . . . . . . . . . . . . . . . . . . . 2.61
Preventive maintenance. . . . . . . . . . . . . . . . . .1.22, 4.1 Signal strength . . . . . . . . . . . . . . . . . . . . . . . . 2.43
Primary AC power switch. . . . . . . . . . . . . . . . . . . .2.5 Sleeves . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.22
Prime . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Snap keys . . . . . . . . . . . . . . . . . . . . . . . . 2.15, 2.42
Prime bag . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.62 Soft tip plunger . . . . . . . . . . . . . . . . . . . . . . . . 3.11
Prime FMS . . . . . . . . . . . . . . . . . . . . . . . . 2.62, 3.4 Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.60
Priming/test sequence. . . . . . . . . . . . . . . . . . . . . .3.4 Sounds. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Probable cause . . . . . . . . . . . . . . . . . . . . . . . . . 5.5 Speakers. . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.4
Procedural step. . . . . . . . . . . . . . . . . . . . . . . . 2.76 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . 1.24
Procedural step buttons . . . . . . . . . . . . . . . . . . . . 2.77 Standby power switch. . . . . . . . . . . . . . . . . 2.4, 3.1, 4.2
Procedure builder dialog . . . . . . . . . . . . . . . . . . . 2.57 Stationary step buttons. . . . . . . . . . . . . . . . . . . . 2.77
Procedure type . . . . . . . . . . . . . . . . . . . . . . . . 2.40 Status panel . . . . . . . . . . . . . . . . . . . . . . . 2.36, 2.64
Product requirements . . . . . . . . . . . . . . . . . . . . . 1.24 Steps. . . . . . . . . . . . . . . . . . . . . . . . 2.57, 2.64, 2.76
Product service. . . . . . . . . . . . . . . . . . . . . . . . 1.22 Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . .4.5
Prv and Nxt navigation keys . . . . . . . . . . . . . . . . . 2.17 Surgery button. . . . . . . . . . . . . . . . . . . . . . . . . 2.63
Pulse phaco mode. . . . . . . . . . . . . . . . . . . . . . . 2.80 Surgery controls. . . . . . . . . . . . . . . . . . . . . 2.64, 2.65
Surgery modes. . . . . . . . . . . . . . . . . . . . . . . . .2.78
R Surgery screen. . . . . . . . . . . . . . . . . . . . . . 2.35, 2.64
Surgery steps . . . . . . . . . . . . . . . . . . . 2.57, 2.64, 2.76
Radio transmitters. . . . . . . . . . . . . . . . . . . . . . . .1.8 Surgery window. . . . . . . . . . . . . . . . . . . . . . . . 2.64
Recommended separation distances . . . . . . . . . . . . . . 1.7 Surgery window with Anterior Vitrectomy step . . . . . . . 2.75
Reconstitution rack . . . . . . . . . . . . . . . . . . . . . . .4.8 Surgery window with AutoSert® step. . . . . . . . . . . . . 2.74
Reflux footswitch button. . . . . . . . . . . . . . . . . . . 3.17 Surgery window with Coagulation step. . . . . . . . . . . . 2.74
Reflux offset. . . . . . . . . . . . . . . . . . . . . . . . . . 2.48 Surgery window with I/A steps. . . . . . . . . . . . . . . . 2.73
Reflux switch . . . . . . . . . . . . . . . . . . . . . . . . . 2.12 Surgery window with Phaco steps . . . . . . . . . . . . . . 2.73
Remote control. . . . . . . . . . . . . . . . . . . . . . . . 2.15 Surgical guidance system. . . . . . . . . . . . . 2.43, 2.50, 2.54
Remote control batteries . . . . . . . . . . . . . . . . . . . 2.17 Surgical settings. . . . . . . . . . . . . . . . . . . . . . . . 2.46
Remote control button. . . . . . . . . . . . . . . . . . . . . 2.42 Symptoms. . . . . . . . . . . . . . . . . . . . . . . . . 5.1, 5.5
Remote control channel. . . . . . . . . . . . . . . . . . . . 2.18 System faults. . . . . . . . . . . . . . . . . . . . . . . . . . 5.3
Remote control communication channel . . . . . . . . . . . 2.53 System messages. . . . . . . . . . . . . . . . . . . . . . . . 5.1
Remote control Enter key. . . . . . . . . . . . . . . . . . . 2.17 System name . . . . . . . . . . . . . . . . . . . . . . . . . 2.54
Remote control keys and buttons. . . . . . . . . . . . . . . 2.15 System power-up. . . . . . . . . . . . . . . . . . . . . . . . 3.1
Remote control Parameter selection button. . . . . . . . . . 2.15 System's configuration . . . . . . . . . . . . . . . . . . . . 2.60
Remote control Parameter Value adjustment keys. . . . . . 2.17 System settings. . . . . . . . . . . . . . . . . . . . . . . . 2.46
Remote control Previous and Next navigation keys . . . . . 2.17 System settings dialog. . . . . . . . . . . . . . . . . . . . .2.53
remote control snap keys . . . . . . . . . . . . . . . . . . . 2.15 System setup . . . . . . . . . . . . . . . . . . . . . . . . . . 3.2
Remove a plunger. . . . . . . . . . . . . . . . . . . . . . . 3.10 System shutdown . . . . . . . . . . . . . . . . . . . . . . . .3.1
Rename doctor . . . . . . . . . . . . . . . . . . . . . . . . 2.38
Rename procedure . . . . . . . . . . . . . . . . . . . . . . 2.40
Replacement items . . . . . . . . . . . . . . . . . . . . . . . 6.1
Reset switch is located in the bottom of the footswitch. . . . .2.8
Restore doctor. . . . . . . . . . . . . . . . . . . . . . . . . 2.56
Retract. . . . . . . . . . . . . . . . . . . . . . . . . . 2.12, 2.85
Retract button. . . . . . . . . . . . . . . . . . . . . . . . . 2.85
Rotating work surface. . . . . . . . . . . . . . . . . . . . . .2.6

7.4
FOR REFERENCE ONLY 8065751772
T Vitrectomy probe . . . . . . . . . . . . . . . . . . . . . . . 1.15
Vitrectomy setup . . . . . . . . . . . . . . . . . 2.89, 3.13, 3.16
Table of contents . . . . . . . . . . . . . . . . . . . . . . . . iii Vitrectomy setup dialog. . . . . . . . . . . . . . . . . . . . 3.13
Task light button . . . . . . . . . . . . . . . . . . . . . . . 2.66 Vit setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.47
Technical service contact information . . . . . . . . . . . . . 5.1 Volume levels. . . . . . . . . . . . . . . . . . . . . . . . . 2.50
Technical Services Department. . . . . . . . . . . . . . xii, 1.22
Telephone. . . . . . . . . . . . . . . . . . . . . . . . . . . . . i W
Test button. . . . . . . . . . . . . . . . . . . . . . . . . . . 3.13
Test chamber . . . . . . . . . . . . . . . . . . . . . . . 2.30, 3.6 Warnings . . . . . . . . . . . . . . . . . . . . xii, 5.1, 5.2, 5.10
Test handpiece. . . . . . . . . . . . . . . . . . . . . . . . . .3.7 Warnings and cautions . . . . . . . . . . . . . . . . . . . . 1.11
Test handpiece button. . . . . . . . . . . . . . . . . . . . . 2.63 Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.23
Test ICD. . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.17 Wi-Fi channel. . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Test ICD Button. . . . . . . . . . . . . . . . . . . . . . . . 2.63 Wi-Fi network. . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Timing configurations. . . . . . . . . . . . . . . . . . . . . 2.79 Wi-Fi region. . . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Tip/Infusion sleeve preparation. . . . . . . . . . . . . . . . .3.6 Wi-Fi SSID . . . . . . . . . . . . . . . . . . . . . . . . . . 2.55
Tips. . . . . . . . . . . . . . . . . . . . . . 1.14, 2.19, 2.21, 6.3 Wireless footswitch. . . . . . . . . . . . . . . . . . . . . . .2.8
Tip with tip holder/wrench. . . . . . . . . . . . . . . . . . 2.30 Wireless signal strength. . . . . . . . . . . . . . . . . . . . 2.43
Tip/Wrench assembly. . . . . . . . . . . . . . . . . . . . . .3.5 Wire loop. . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3
Toe switch control. . . . . . . . . . . . . . . . . . . . . . . 2.11 Work surface . . . . . . . . . . . . . . . . . . . . . . . . . . 2.6
Tones . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.4, 2.50
Tones . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.18
Torsional amplitude. . . . . . . . . . . . . . . . . . . . . . 2.78
Touch screen . . . . . . . . . . . . . . . . . . . . . . . . . 2.35
Touch Screen. . . . . . . . . . . . . . . . . . . . . . . . . . 2.3
Tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2.3
Tray support cover . . . . . . . . . . . . . . . . . . . . . . 2.30
Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . .5.1
Troubleshooting Guide . . . . . . . . . . . . . . . . . . . . .5.4
TurboSonics® family of tips. . . . . . . . . . . . . . . . . . 2.21

UltraChopper® tip. . . . . . . . . . . . . . . . . . . . . . . 2.21

Ultraflow™* II I/A handpiece . . . . . . 1.15, 2.23, 3.2, 3.9, 6.4
Ultra infusion sleeves. . . . . . . . . . . . . . . . . . . . . 2.22
UltraVit® anterior vitrectomy probe. . . . . . . . . . . .2.26, 6.5
UltraVit® probe setup . . . . . . . . . . . . . . . . . . 3.13, 3.16
Universal precautions. . . . . . . . . . . . . . . . . . . . . .1.4
USB communications. . . . . . . . . . . . . . . . . . . . . .2.5
USB removable media (flash drive). . . . . . . . . . . . . . 2.56
U/S tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.21
U/S tip/wrench assembly . . . . . . . . . . . . . . . . . . . .3.5
Utility light. . . . . . . . . . . . . . . . . . . . . . . . . . . 2.3

Vacuum . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.3
Vacuum adjustments . . . . . . . . . . . . . . . . . . . . . 1.16
Vacuum control . . . . . . . . . . . . . . . . . . . . . . . . 2.83
Vacuum range for I/A tips. . . . . . . . . . . . . . . . . . . 1.15
Vacuum rise. . . . . . . . . . . . . . . . . . . . . . . . . . 2.72
Vacuum settings. . . . . . . . . . . . . . . . . . . . . . . . 2.71
Vacuum test. . . . . . . . . . . . . . . . . . . . . . . . . . .3.4
Vacuum threshold. . . . . . . . . . . . . . . . . . . . . . . 2.67
Vacuum tone. . . . . . . . . . . . . . . . . . . . . . . . . . 1.18
Vent test. . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.4
Vent time adjustment. . . . . . . . . . . . . . . . . . . . . 2.49
Verify PEL. . . . . . . . . . . . . . . . . . . . . . . . 2.47, 2.63
VideOverlay. . . . . . . . . . . . . . . . . . . . . . . . . . 2.31
VideOverlay output (RS232) . . . . . . . . . . . . . . . . . .2.5
VideOverlay system. . . . . . . . . . . . . . . . . . . . . . 1.20
Visco aspiration (Visco Asp). . . . . . . . . . . . . . . . . 2.92
Vit cutter button dual assignment. . . . . . . . . . . . . . . 2.49
Vit port . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.13
Vitrectomy cutter . . . . . . . . . . . . . . . . . . . . . . . 2.89
Vitrectomy mode of operation . . . . . . . . . . . . . . . . 2.89

8065751772 7.5
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7.6
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REFERENCE
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