GE Mac-Lab_CardioLab_Centricity Cardiology INW Service Manual_SM_2088535-010_F Centricity Cardiology INW Service Manual Software Version 6.9.6 R2 2088535-010F EN

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GE Healthcare

Mac-Lab/CardioLab/ Centricity Cardiology INW Service Manual

Software Version 6.9.6 R2

2088535-010F EN

Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

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Publication Information

The information in this manual only applies to Mac-Lab/CardioLab/Centricity Cardiology INW software version

6.9.6 R2. It does not apply to earlier software versions. Due to continuing product innovation, specifications in this manual are subject to change without notice.

†

Mac-Lab, CardioLab, Centricity, CardioICE, DASH, Innova, Solar, TRAM, TRAMNet, TRAM-RAC and Vivid are

all trademarks of GE Healthcare companies.

††

All third party trademarks are the property of their respective owner.

Micropace digital stimulators are sold by GE Healthcare for Micropace EP Inc.

GE Healthcare, a division of General Electric Company

GE and the GE Monogram are trademarks of General Electric Company.

This product complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices.

Rx Only

The document number and revision appear on the bottom of each page. The following table outlines the changes applied with each revision.

Revision Date Comment

A 23 September 2015 Internal release.

B 17 January 2016 Initial public release.

C 12 May 2016 Added information for new HP printers.

Added information for Blood Pressure Cover. Updated the Blood Pressure Connector Kit part number in the Amplifier Parts List. Removed Workstation Desk part numbers from Parts List and Physical Dimensions tables.

T-2 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

30 November 2018

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Revision Date Comment

D 21 June 2017 Updated International Power Cords table.

E 4 December 2017 Added supported PDM peripheral devices.

Updated z440 replacement parts for fans, the power supply, and the SD reader drive and cable. Updated TRAMNet board part number. Removed PN 2006323-001 CABLE POWER, IEC C19 TO UNTERMINATED, from the IEB Replacement Parts List in Chapter 6. Removed PDM accessories from Appendix E. Renamed Appendix E to "PDM Battery." Updated Masimo finger sensor part numbers in Chapter 6. Updated preventative maintenance frequency information.

F 30 November 2018 Updated for IEC/EN 60601-1-2 4th ed.

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual T-3

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T-4 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

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Contents

1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1

Manual Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Product References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Printed Copies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Operators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

System Administrator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Field Service Engineer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Indications for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Types Of Systems. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Mac-Lab System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4

CardioLab System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4

ComboLab System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5

SpecialsLab System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5

Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5

Classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6

Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8

Illustrations and Names . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8

Related Documents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8

Safety Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9

Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9

Applicable Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-10

Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

Responsibility of the User . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

Anti-Virus Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

Product Vulnerability and Security Patches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-18

Equipment Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-18

2 Equipment Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1

Serial Number Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

Typical Acquisition System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3

Control Room Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4

Procedure Room Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5

IT Control Room Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6

Network Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6

Review Workstations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

Nurse's Workstation Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual i

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Remote Review Workstation Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

Pre/Post Review Workstation Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

Supported Peripheral Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8

System Hardware . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9

Acquisition System Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9

Uninterruptible Power Supply (UPS). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-24

Review Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25

External Components and Connections for the Review Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26

Mobile Workstand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-27

Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-28

Patient Data Module (PDM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-29

Analog Out and Defib/Sync. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30

PDM Base Station . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-31

PDM Base Station Plus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-31

PDM and Base Station Mounting Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-32

TRAMNet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-35

RAC 4A . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-36

CardioLab II Plus Amplifier. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-36

Front View. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-37

Back View of Amplifier – Generic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39

CardioLab II Plus Catheter Input Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-40

Equipotential Grounding Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-41

Accessory Parts List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42

CARTO System (Patient Interface Unit) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-44

Analog Output Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46

Network Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47

Centricity Cardiology INW G9 Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47

Cabling and Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-49

HP z440 Computer I/O Backplane Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-49

Power Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-50

HP z440 Video Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-51

Communications Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-52

TRAM/Amplifier Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-53

PDM/Amplifier Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-54

PDM Base Station Plus/CO2 Connections. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-55

Typical Setup (with Capnostat 5 Mainstream CO2 Sensor) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-55

Typical Setup (with LoFlo Sidestream CO2 Module) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-56

Amplifier/Stimulator Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-57

Typical Setup (with MicroPace) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-57

Typical Setup (with Bloom) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-58

Equipment Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-59

Bloom (Connection Detail) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-60

Audio . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-61

CARTO 3 System Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-62

Vivid Connections - CardioLab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-65

Vivid Connections - Mac-Lab with TRAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-66

Vivid Connections - Mac-Lab with PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-67

CARTO/CardioLab/Vivid Integration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-68

Review Workstations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-69

Review Workstation Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-69

Solar Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-70

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DASH Connection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-71

Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-72

Operating System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-72

Database . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-72

Application Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-72

3 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Powering on the Acquisition System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Powering on the Review Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4

Initial Troubleshooting Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4

Hardware . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5

Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-28

GEMS Task Monitor Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-31

Networking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-31

Normal Operation and Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32

IP Address . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32

Slow Transfer/Ping Speed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32

DNS: Client Side . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33

DNS: Server Side . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33

Centricity Cardiology INW Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33

Operation and Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33

CVIS and DICOM Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-35

Normal Operation and Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-35

Test DICOM Connectivity (CVIS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-37

HL7 Export to CVIS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-38

Test DICOM Connectivity (X-Ray or Ultrasound) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-40

INNOVA CENTRAL/Touch Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-41

Check Connection Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-41

CARTO 3 System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-42

Normal Operation and Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-42

CARTO System Button Inactive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-42

CARTO System Connection Failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-43

CARTO IP Address Conflict . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-43

Cannot Print to CARTO Printer from Acquisition System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-43

Mapping Points are Unsynchronized or Missing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-43

Network Irregularity Error with CARTO System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-43

Data Import Does Not Work for Non-English Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-44

EP Recording is Disabled on the CARTO System . . . . . . . . .

Send Movies Option Disabled in EP Recording Preferences on the CARTO System . . . . . . . . . . . . . . . . 3-45

Vivid System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

Error Messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

Force Time Synchronization with Vivid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

EtCO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

Capnostat Sensor Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

General Error Messages - ETCO2 with TRAM RAC. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-46

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-44

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual iii

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General Error Messages - ETCO2 with PDM Base Station Plus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-48

Remote Connectivity - InSite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-49

Normal Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-49

Start/Stop InSite Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-49

FastPoll - Initiate Remote Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-50

Log Files. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-53

Event Viewer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-54

Application Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-54

Device Log Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-55

Install/Update Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-57

Maintenance Log Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-57

Log File Locations for Mac-Lab/CardioLab System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-58

Corrupted or Missing Operator’s Manual Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-58

Event Log Collection from the Centricity Cardiology INW Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-59

4 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1

Mac-Lab/CardioLab Service Performance Testing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2

FRU Checkout Procedure Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3

Tools Recommended . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5

Visual Inspection/Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5

Mac-Lab/CardioLab System Electrical Safety Testing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6

Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6

Test Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7

Test Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7

Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8

Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8

Checkout Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-22

Mac-Lab SCOP (Standard Checkout Procedure) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-22

CardioLab SCOP (Standard Checkout Procedure) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-24

TRAM Module Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

PDM Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

CO2 Module Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

CO2 Module with PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

Capnostat/Capnoflex with TRAM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26

CardioImage/Image Capture Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

IEB Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

Printer Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

CARTO Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

Audible Indicators Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27

RF Ablation Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-28

Stimulator Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-28

DASH / Solar Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-28

Remote Operators Terminal Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-28

Analog Out Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-29

Centricity Cardiology INW Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-29

Remote Connection Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-31

Planned Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

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General Cleaning and Inspection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

General Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

General Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-32

Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-33

Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

Clean CRT Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

Clean LCD Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-34

Mac-Lab Leadwires and ECG Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36

Sterilize Leadwires and ECG Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36

CardioLab Leadwires and ECG Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36

Catheter Input Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-37

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-37

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-37

CardioLab II Plus Amplifier. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-38

Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-38

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-38

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-38

Blood Pressure Connector Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

IEB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

Clean IEB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

Inspect IEB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

Safety Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39

Function Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-40

RF Filter Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41

Analog Output Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-42

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-42

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-42

System Interconnect Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-43

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-43

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-43

Computer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Clean Computer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Inspect Computer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Preventative Part Replacement Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Boot Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-44

Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-45

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-45

Clean Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-45

Inspect Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-45

Preventative Part Replacement Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-45

Vivid External Trackball . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-47

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-47

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-47

Inspecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-47

Performance Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-48

Vivid Mount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-49

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-49

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Cleaning and Disinfecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-49

Printer Planned Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-50

Tools and Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-50

Uninterruptible Power Supply (UPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-51

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-51

Clean Uninterruptible Power Supply (UPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-51

Inspect Uninterruptible Power Supply (UPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-51

Preventative Part Replacement Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-52

Mobile Workstation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-53

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-53

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-53

Adjusting Tilt and Tilt Tension. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-53

Adjusting Swivel or Pivot Tension . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-54

Routine Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-54

Desk . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-54

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-54

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-54

PDM Base Station, PDM Base Station Plus. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-55

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-55

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-55

PDM Base Station Mount. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-56

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-56

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-56

PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-56

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-56

Visual Inspection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-57

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-57

Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-57

Consequences of Using Improper Cleaning Product . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-58

Cleaning Products to Avoid. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-58

Expansion Cover Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-58

Battery Compartment Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-58

PDM Bedrail/Mount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-59

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-59

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-59

Stimulator Cable. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-59

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-59

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-60

Ablation Stim Extender Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-61

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-61

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-61

Auxiliary Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

Capnoflex LF CO2 Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

PDM CO2 Modules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

Other GE Peripheral Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-62

OEM Component Support Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-64

Disk Defragmentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-65

Defragmentation Scheduling Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-65

Centricity Cardiology INW Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-65

Acquisition System/Review Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-66

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5 EIZO Monitor Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

Monitor Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

Before You Begin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Reset all Monitor Settings to Default . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Turn Off Automatic Brightness Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Adjust Screen Using Pattern Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Select Display Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5

Adjust Color Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6

Adjust Brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6

Adjust Color Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6

6 Parts List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1

HP z440 Computer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

Integrated Electronics Box (IEB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5

Uninterrupted Power Source (UPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7

Review Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8

DASH Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10

Solar Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10

Centricity Cardiology INW G9 Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-11

PDM and PDM Base Station . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12

Cables and Mounting Hardware . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12

TRAMNet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-13

Amplifier . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14

Vivid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-15

MicroPace . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16

RMOT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16

Speakers and Miscellaneous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17

Ablation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17

Analog Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17

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CARTO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17

Speakers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18

CO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18

Desks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19

International Power Cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19

Monitors and Printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-22

A Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1

Electrical and Product Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-2

Miscellaneous Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4

B Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-1

Electrical Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2

Atmospheric Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3

Intracardiac ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3

Physical Dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3

Validated Third Party Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-5

C Electromagnetic Compatibility (EMC) and Electromagnetic Disturbances (EMD)

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-2

Electromagnetic Immunity Pass/Fail Criteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2

Guidance and Manufacturer’s Declaration - Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-2

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-3

Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-4

Electromagnetic Disturbances (EMD) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-6

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-6

D Maintenance Record of Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-1

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-2

IEB Maintenance Record of Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-3

Computer Maintenance Record of Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-4

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-4

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-4

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Server Maintenance Record of Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-5

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-5

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-5

Vivid External Trackball Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-6

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-6

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-6

Printer Maintenance Record of Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-7

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-7

Uninterruptible Power Supply (UPS) Maintenance Record of Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-8

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-8

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-8

PDM and PDM Base Station Maintenance Record of Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-9

Maintenance Record – PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-9

Maintenance Record – PDM Base Station/PDM Base Station Plus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-9

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-9

Mobile Workstand Maintenance Record of Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-11

Maintenance Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-11

Equipment Table and Tester Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-11

Electrical Safety Test Results Record. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-12

Protective Earthing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-13

Earth Leakage Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-14

Enclosure Leakage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-15

Patient (Source) Leakage Current — CardioLab II Plus Amplifier . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-17

Patient (Sink) Leakage Current — CardioLab II Plus Amplifier . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-17

Patient (Source) Leakage Current — PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-17

Patient (Sink) Leakage Current — PDM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-18

E PDM Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-1

PDM Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Battery Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Storage Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Battery Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Charging the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Testing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-2

Replacing the Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-3

Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-3

Replace the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-3

Recycling the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-4

F EU Battery Directive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-1

EU Battery Directive 2006/66/EC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-2

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x Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

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Chapter 1

Introduction

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Introduction

Manual Information

Purpose

This manual contains the instructions necessary to operate and service the Mac-Lab/CardioLab

and/or Centricity Cardiology INW system safely in accordance with its function and intended use.

These instructions include but are not limited to:

 Describing fundamental controls and indicators

 Operating procedures

 Connecting and disconnecting detachable parts and accessories

 Troubleshooting and service procedures

Product References

The name of the product described in this manual is Mac-Lab/CardioLab. It will also be referred to

as “the system” throughout this manual.

Printed Copies

Contact your local GE representative to request a paper copy of this manual.

Intended Audience

This manual is written for trained GE Healthcare Field Service Engineers and hospital Biomedical

Technicians who use, maintain, troubleshoot, and service the Mac-Lab/CardioLab system. Service

professionals are expected to have a working knowledge of appropriate medical, electrical, and

mechanical procedures, practices and terminology used in the service of the equipment.

Operators

 Operators can record and calculate cardiovascular data from pediatric or adult patients as they

undergo cardiac catheterization. Cardiovascular data may be manually entered or acquired via interfaced GE Healthcare TRAM/PDM modules or other interfaced systems.

 The Mac-Lab/CardioLab operator requires training to become familiar with the capabilities and

operations of the Mac-Lab/CardioLab system. The following training options are available:

 Classroom training at GE Healthcare Institute in Milwaukee, WI

 On-site customer training

 Video training via weblink

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System Administrator

 Coordinating the overall Mac-Lab/CardioLab system is the responsibility of the System

Administrator. This person has access to additional system supervisory functions, including operational setup parameters, system backup functions, for example.

 The System Administrator is also responsible for monitoring and reporting system hardware

and software problems using the procedures described in the Mac-Lab or CardioLab operator manual.

 The Mac-Lab/CardioLab System Administrator should be familiar with the Windows desktop

and be fully trained on the Mac-Lab/CardioLab features and configuration settings.

NOTE: A System Administrative password is required to perform any of the previous

administrative functions.

 The Mac-Lab/CardioLab System Administrator requires training to become familiar with the

capabilities and operations of the Mac-Lab/CardioLab system. The following training options are available:

 Classroom training at GE Healthcare Institute in Milwaukee, WI

 On-site customer training

Introduction

Field Service Engineer

Diagnosing and correcting problems with the Mac-Lab/CardioLab system must be done by a

trained GE Healthcare Field Service Engineer. Please refer system problems not covered in this

manual to GE Healthcare Product Support.

Indications for Use

Types Of Systems

The following system names are used:

 Mac-Lab is a Hemodynamic Recording System.

 CardioLab is an Electrophysiology Recording System built on a common platform with

Mac-Lab.

 ComboLab is a single system that contains the features of both the Mac-Lab and the

CardioLab systems.

 SpecialsLab is a system with a subset of the features available on the Mac-Lab.

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Introduction

Mac-Lab System

The Mac-Lab System is intended for acquiring, filtering, digitizing, amplifying, measuring and

calculating, displaying, recording and monitoring of clinical data from adult and pediatric patients.

Clinical data may include: ECG waveforms, heart rate, pulse oximetry (SpO

(EtCO2), temperature, hemodynamic measures (for example, valve gradients and areas,

cardiac output, shunts, Fractional Flow Reserve (FFR), invasive and noninvasive blood pressure).

Physiology parameters such as diastolic, systolic, and mean pressures, and heart rate may be

derived from the signal data, displayed and recorded. The data may be entered manually or

acquired via interfaced devices and/or information systems and may be used for report generation.

Procedural information and optional anatomical and physiological imaging and data devices may

be interfaced (for example, X-ray, ultrasound, patient monitors and information systems). The

Mac-Lab System can display, store and annotate images previously acquired and stored by other

systems. Data may be provided to other systems via multiple formats (for example, HL7, DICOM,

Analog outputs). Data may be received from other devices via multiple formats (for example,

DICOM, Analog inputs).

Optional accessories for hardware and software may include research tools to be used exclusively

outside patient care settings. The purpose of the research tools is to assist researchers or

clinicians in developing algorithms.

), respiration rate,

The Mac-Lab System does not have alarms, does not generate energy delivered to the patient,

does not administer drugs and does not perform any life-supporting or life-sustaining functions.

The Mac-Lab System is not intended for use on unattended patients, or in situations where

diagnostic arrhythmia detection is required.

The Mac-Lab System provides the ability to transmit patient data for storage, analysis and viewing

at distributed locations within a clinical facility via network connectivity. The Mac-Lab System may

also function as a stand-alone device. The Mac-Lab System is used in a variety of hospital and

clinical settings including interventional laboratories (for example, cardiac catheterization and

radiology), operating room environments, and pre and post areas all under the direct supervision

of licensed healthcare practitioners who are responsible for interpreting the data.

CardioLab System

The CardioLab System is intended for acquiring, filtering, digitizing, amplifying, measuring and

calculating, displaying, recording and monitoring of clinical data from adult and pediatric patients.

Clinical data may include: ECG waveforms, intracardiac signals, stimulus data, ablation data,

pulse oximetry (SpO

blood pressure. Physiological parameters such as diastolic, systolic, and mean pressures, heart

rate, and cycle length may be derived from the signal data, displayed and recorded. The data may

be entered manually or acquired via interfaced devices and/or information systems and may be

used for report generation.

Procedural information and optional anatomical and physiological imaging and data devices may

be interfaced [for example, X-ray, ultrasound, mapping systems, ablation generators (for example,

RF and cryogenic), simulators, patient monitors and information systems]. The CardioLab System

can display, store and annotate images previously acquired and stored by other systems. Data

may be provided to other systems via multiple formats (for example, HL7, DICOM, Analog

outputs). Data may be received from other devices via multiple formats (for example, DICOM,

Analog inputs).

), respiration rate, CO2 (EtCO2), temperature, and invasive and noninvasive

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Optional accessories for hardware and software may include research tools to be used exclusively

outside patient care settings. The purpose of the research tools is to assist researchers or

clinicians in developing algorithms.

Optional accessories for hardware and software may also include a waveform simulator to be

used exclusively outside patient care settings. The waveform simulator may be used for training,

demonstration without a patient attached, and as a troubleshooting tool in the CardioLab System.

The CardioLab System does not have alarms, does not generate energy delivered to the patient,

does not administer drugs and does not perform any life-supporting or life-sustaining functions.

The CardioLab System is not intended for use on unattended patients, or in situations where

diagnostic arrhythmia detection is required.

The CardioLab System provides the ability to transmit patient data for storage, analysis and

viewing at distributed locations within a clinical facility via network connectivity. The CardioLab

System may also function as a stand-alone device. The CardioLab System is used in a variety of

hospital and clinical settings including interventional laboratories (for example, electrophysiology

and cardiac catheterization), operating room environments, and pre and post areas all under the

direct supervision of licensed healthcare practitioners who are responsible for interpreting the

data.

ComboLab System

Introduction

The ComboLab System is the combination of both the Mac-Lab and CardioLab Systems. The

ComboLab System allows the user to run either the Mac-Lab System or the CardioLab System,

although only one system may be used at a time. The ComboLab System executes the same

software and runs on the same hardware in the same environments as the Mac-Lab and

CardioLab Systems.

SpecialsLab System

The SpecialsLab System executes the same software and runs on the same hardware in the same

environment as the Mac-Lab System. Products designated as a SpecialsLab System support

fewer options than the Mac-Lab system.

Compliance

The system complies with the following standards:

 IEC/EN 60601-1 2nd ed Medical Electrical Equipment, Part 1 General Requirements for

Safety

 IEC/EN 60601-1 3rd ed Medical Electrical Equipment, Part 1 General Requirements for Basic

Safety and Essential Performance

 IEC/EN 60601-1 3rd ed (Amendment 1) Medical Electrical Equipment, Part 1 General

Requirements for Basic Safety and Essential Performance

 IEC/EN 60601-1-1 Safety requirements for medical electrical systems

 IEC/EN 60601-1-2 Electromagnetic compatibility - Requirements and tests

 IEC/EN 60601-1-2 4th ed Electromagnetic disturbances - Requirements and tests

 IEC/EN 60601-1-4 Programmable electrical medical systems

NOTE: Upgrade systems may not comply with IEC/EN 60601-1 3rd ed and IEC/EN 60601-1 3rd

ed (Amendment 1).

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 1-5

Page 20

Introduction

US-only Mac-Lab/CardioLab systems comply with the following standards:

 IEC/EN 60601-1 2nd ed Medical Electrical Equipment, Part 1 General Requirements for

Safety

 IEC/EN 60601-1 3rd ed Medical Electrical Equipment, Part 1 General Requirements for Basic

Safety and Essential Performance

 IEC/EN 60601-1 3rd ed (Amendment 1) Medical Electrical Equipment, Part 1 General

Requirements for Basic Safety and Essential Performance

 IEC/EN 60601-1-1 Safety requirements for medical electrical systems

 IEC/EN 60601-1-2 Electromagnetic compatibility - Requirements and tests

 IEC/EN 60601-1-2 4th ed Electromagnetic disturbances - Requirements and tests

 IEC/EN 60601-1-4 Programmable electrical medical systems

Classification

This system is classified according to IEC 60601-1 as follows:

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Introduction

shock

Type of protection against electrical

Degree of protection against electrical

IEB Class I N/A

CardioLab II Plus Amplifier:

Class I

CF Defib Proof ECG, IBP, IC ECG, Auxiliary

PDM Base Station Class I N/A

PDM Base Station Plus Class I BF

PDM

ECG, IBP, SpO

NBP

, Temp, CO

Class I

CF Defib Proof

BF Defib Proof

TRAM-RAC Class I N/A

TRAM module:

ECG, IBP, SpO

NBP

, Temp, CO

Class II CF Defib Proof

BF Defib Proof

shock

ingress of water

Degree of protection against harmful

nitrous oxide

Mode of Operation

mixture with air or with oxygen or

presence of a flammable anesthetic

Degree of safety of application in the

Ordinary

IPX1

Not Suitable Continuous

Capnostat Mainstream CO

CapnoFlex CO

module

PDM Base Station Plus LoFlo Sidestream CO module

PDM Base Station Plus CAPNOSTAT 5 Mainstream CO

sensor

module

N/A BF

Vivid Remote Trackball N/A N/A

Ordinary

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Introduction

Conventions

The following conventions are used throughout this manual.

Bold Indicates keys on the keyboard, text to be entered or hardware items such as buttons or switches

on the equipment.

Italics Indicates software terms that identify menu items, buttons or options in various windows.

[Key1] + [Key2] Indicates a keyboard operation. A (+) sign between the names of two keys means press and hold

Enter Press the “Enter” or “Return” key on the keyboard. Do not type “enter”.

the first key while pressing the second key once.

For example, “Press Ctrl + Esc” means to press and hold down the Ctrl key while pressing the Esc key.

Illustrations and Names

All illustrations in this manual are provided as examples only. They may not necessarily reflect the

setup or the data on your system.

In this manual, all names appearing in examples and illustrations are fictitious. The use of any real

person's name is purely coincidental.

Safety Information

Read through the following safety information before putting the system into use. Disregarding

information on safety is considered abnormal use.

The terms danger, warning and caution are used throughout this manual to point out hazards and

to designate a degree or level of seriousness.

Definitions

Hazard is defined as a source of potential injury to a person.

DANGER: IMMINENT DEATH OR SERIOUS INJURY

Danger messages indicate an imminently hazardous situation which, if not avoided, will result in death or serious injury.

Introduction

General

WARNING: POTENTIAL DEATH OR SERIOUS INJURY

Warning messages indicate a potentially hazardous situation which, if not avoided, may result in death or serious injury.

CAUTION: POTENTIAL INJURY OR EQUIPMENT DAMAGE

Caution messages indicate a potentially hazardous situation which, if not avoided, may result in minor to moderate injury or equipment damage.

NOTE: Notes provide additional user information.

WARNING: UNSUPERVISED USE

This device is intended for use under the direct supervision of a licensed health care practitioner.

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Introduction

WARNING: This system is designed to comply with the applicable IEC/EN 60601-1 series

safety standards when connected and powered as specified. Connecting additional devices, parts or accessories that are not recommended by GE Healthcare could lead to a reduced level of safety. Refer to the Service Manual for equipment connection and service information. Contact GE Healthcare if questions arise.

WARNING: Before connecting supported interfaced devices to the system, ensure that the

devices meet the requirements of the applicable IEC 60601 series safety standards and the system configuration meets the requirements of the IEC 60601-1-1 medical electrical systems standard.

Applicable Messages

DANGER: EXPLOSION HAZARD

Using this equipment in the presence of flammable gases (including anesthetics and oxygen) may cause an explosion or fire. Always use this equipment in a well ventilated area away from the presence of potentially flammable gases.

WARNING: The use of unspecified accessories, transducers and cables may result in

increased emissions or decreased immunity of the system.

WARNING: Use of accessories, transducers and cables other than those specified or

provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.

WARNING: The Mac-Lab, CardioLab, ComboLab, and SpecialsLab systems are not

intended to be used together with high-frequency surgical equipment. The combined use may result in decreased immunity of the Mac-Lab, CardioLab, ComboLab, and SpecialsLab system.

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Introduction

WARNING: Portable RF communications equipment (including peripherals such as

antenna cables and external antennas) should be used no closer than 30 cm (12 in) to any part of the Mac-Lab, CardioLab, ComboLab, and SpecialsLab systems, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

WARNING: Use caution when cleaning the environment near equipment. Fluid ingress may

damage devices or compromise electrical safety.

WARNING: Modify equipment only as authorized by the manufacturer. After modifications,

appropriate inspection and testing must be conducted to ensure continued safe use of the equipment.

WARNING: ELECTRICAL HAZARDS

Connect equipment only as specified in the cabling diagrams. Failure to do so may lead to increased electrical safety risk.

WARNING: ELECTRICAL HAZARD

Power equipment only as specified. Do not connect equipment to extension cords or multiple socket outlets.

WARNING: EQUIPMENT FAILURE

System components should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the system should be observed to verify normal operation in the configuration in which it will be used.

WARNING: EQUIPMENT FAILURE

Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.

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Introduction

WARNING: EQUIPMENT HAZARD

Route cables through floor or ceiling conduit wherever possible. Ensure the fiber optic cable is protected from potential sources of damage.

WARNING: EQUIPMENT HAZARD

Do not attempt to service the UPS or replace the battery. Doing so could result in equipment damage. Contact qualified GE Service personnel for service or replacement.

WARNING: EXPLOSION HAZARD

Do not incinerate the UPS battery or store at high temperatures.

WARNING: FALLING EQUIPMENT

Do not place the PDM more than 147 cm (58 in) from the floor when mounting on an IV pole with a base less than 58 cm (23 in) in diameter. This may cause the IV pole to tip over.

WARNING: FALLING EQUIPMENT

Monitor suspension systems other than the Mavig GD60 Series have not been validated for remote monitors.

WARNING: SYSTEM INSTABILITY

DO NOT load any software or patches other than those specified by GE Healthcare onto the system. Doing so may result in system instability or failure.

WARNING: SHOCK HAZARD

Do not power unspecified devices from the system equipment outlets.

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Page 27

WARNING: SHOCK HAZARD

If liquids or foreign materials have entered a device, take it out of service and have it checked by qualified service personnel to verify safety and functionality before it is used again. Ingress of foreign substances may result in shock, fire, excess leakage current, or device failure.

WARNING: SHOCK HAZARD

To ensure patient safety, all equipment connected to the system must be powered from an isolated power source.

WARNING: SHOCK HAZARD

To reduce the risk of electric shock or damage to equipment, the equipment must only be connected to a properly installed power outlet with protective ground contacts.

Introduction

WARNING: SHOCK HAZARD

To reduce the risk of shock and equipment damage, use safe working practices when servicing electrical equipment.

WARNING: SHOCK HAZARD

Damaged cables and loose connections present a shock hazard and could cause signal noise or impaired device operation. Ensure all cables are in good condition and securely connected before powering on equipment. Replace damaged cables immediately.

WARNING: SHOCK HAZARD

Use caution when cleaning the environment near equipment. Fluid ingress may damage devices or compromise electrical safety.

WARNING: SHOCK HAZARD

Do not connect analog input or analog output cables to patient-isolated equipment interfaces. This could compromise patient safety.

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Introduction

WARNING: SHOCK HAZARD

The Patient (sink) Leakage Current test causes high voltages on the test body. Do not touch conductive regions of the safety analyzer.

WARNING: SHOCK HAZARD

To fully isolate the equipment from mains power, disconnect the power cord from the mains supply.

WARNING: SHOCK HAZARD

To reduce the risk of ingress of water into the equipment, do not mount the PDM in a vertical position with the patient cables facing up or down.

WARNING: SHOCK HAZARD

The CardioLab II Plus amplifier defibrillation protection is only guaranteed when approved accessories are used. Do not use unspecified accessories.

WARNING: SYSTEM INSTABILITY

Do not install or use unvalidated anti-virus software (including unvalidated versions). Doing so may result in system instability or failure. Use only validated anti-virus software in the appropriate language version.

WARNING: SYSTEM INSTABILITY

Do not install any third party software onto the system, unless specified by GEHealthcare. Doing so may result in system instability or failure.

WARNING: TIPPING HAZARD

Do not attempt to transport the Mobile Workstand while the wheels are locked.

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Page 29

WARNING: TRIPPING HAZARD

Keep cables away from accessible walkways. Failure to do so may present a tripping hazard and could result in cable damage.

CAUTION: EQUIPMENT DAMAGE

Swivel tension nut on the Mobile Workstand must be torqued to a minimum of 20 in-lbs [2.3 N-m].

CAUTION: EQUIPMENT DAMAGE

Tilt tension screws on the Mobile Workstand must be torqued to a minimum of 35 in-lbs [4.0 N-m].

Introduction

CAUTION: EQUIPMENT DAMAGE

Do not use benzene, thinner, ammonia, or any other volatile substances to clean the monitor or the screen. These chemicals may damage the cabinet finish as well as the screen.

CAUTION: EQUIPMENT DAMAGE

Do not use OA cleaner as it will cause deterioration or discolor the LCD surface.

CAUTION: LOSS OF FUNCTION

Do not edit or change the original dcf files. They may be needed in the future. Always create a copy of the original dcf file to work on.

CAUTION: SYSTEM FAILURE

To ensure an adequate system power supply, GE Healthcare recommends using a dedicated circuit to power the IEB.

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Introduction

CAUTION: SYSTEM INSTABILITY

All networked systems at a location must be on the same version of Mac-Lab/ CardioLab software. Failure to do so may result in slowed performance, data corruption, or system instability.

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Page 31

Responsibility of the Manufacturer

GE Healthcare is responsible for the effects of safety, reliability and performance only if:

 Assembly operations, extensions, readjustments, modifications or repairs are carried out by

persons authorized by GE Healthcare.

 The electrical installation of the relevant room complies with the requirements of the

appropriate regulations.

 The equipment is used in accordance with the instructions for use.

Responsibility of the User

General

Keep this manual with the equipment at all times. Periodically review this manual for information

regarding system operation. If further assistance is required, contact GE Healthcare.

Anti-Virus Software

Introduction

The following should be noted regarding the use of anti-virus software. Refer to the Mac-Lab/

CardioLab Security Guide (PN 2088535-004) for further information.

 Anti-virus software is not provided with the Mac-Lab/CardioLab system and it is the customer’s

responsibility to acquire, install and maintain.

 The customer is responsible for updating anti-virus definition files.

 If a virus is found, contact the facility System Administrator and GE Technical Support.

 The anti-virus software used must be one that has been validated by GE Healthcare.

 The language version of the anti-virus software must match the operating system language.

Product Vulnerability and Security Patches

Customers are responsible to stay informed on the Mac-Lab/CardioLab product vulnerability

status and the installation of validated security patches for the Mac-Lab/CardioLab systems. Refer

to the Mac-Lab/CardioLab Security Guide (PN 2088535-004) for further information.

Preventative Maintenance

It is the responsibility of the user to properly maintain the system equipment. Refer to Maintenance

on page 4-1 in this manual and the accompanying service manual for further information.

Failure on the part of the responsible individual, hospital or institution using this equipment to

implement a satisfactory maintenance schedule may cause undue equipment failure and possible

health hazards.

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Introduction

Service

WARNING: EQUIPMENT FAILURE

Failure on the part of all responsible individuals, hospitals or institutions, employing the use of this device, to implement the recommended maintenance schedule may cause equipment failure and possible health hazards. The manufacturer does not, in any manner, assume the responsibility for performing the recommended maintenance schedule, unless an Equipment Maintenance Agreement exists. The sole responsibility rests with the individuals, hospitals, or institutions utilizing the device.

Regular maintenance, irrespective of usage, is essential to ensure that the Mac-Lab/CardioLab

system will always be functional when required. In the event that service is needed for the

equipment, contact your GE Healthcare service representative.

Refer equipment servicing to GE Healthcare authorized service personnel only. Any unauthorized

attempt to repair equipment under warranty voids that warranty.

Any unauthorized attempt to install third-party software on a system under warranty, voids that

warranty.

It is the user’s responsibility to report the need for service to GE Healthcare or to one of their

authorized agents.

Equipment Symbols

Equipment Symbols Descriptions

RX Only CAUTION: U.S. federal law restricts this device to sale by or on the order of a physician.

CE Marking

Compliance with applicable EU (European Union) directives.

Russia only. GOST-R mark.

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Page 33

Equipment Symbols Descriptions

Underwriters Laboratories, Inc.

Non-US Systems:

Medical – general medical equipment as to electrical shock, fire and mechanical hazards only in accordance with UL60601-1, CAN/CSA C22.2 No. 601.1, ANSI/AAMI ES60601-1 (2005, 3rd ed.), AND CAN/CSA-C22.2 No. 60601-1 (2008).

US-Only Systems:

Classified by Underwriters Laboratories Inc. with respect to electric shock, fire, mechanical and other specified hazards, only in accordance with UL 2601-1, CAN/CSA C22.2 No. 601.1, IEC 60601-1 and IEC 60601-1-1.

WEEE

Indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.

WEEE

The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements (Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all devices with batteries are properly recycled or disposed.

Introduction

Information on the potential effects on the environment and human health of the substances used in batteries is available at this url:

http://www.gehealthcare.com/euen/weee-recycling/index.html

Fuse

Equipotential Ground Point

A nonessential electrical connection which may be used to connect the chassis to other equipment to achieve the same potential.

Standby

Mains Power Switch

1 is on. 0 is off.

Insert SD

Indicates that the computer has an SD drive located near this symbol.

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Introduction

Equipment Symbols Descriptions

Insert SD Here

Type CF Equipment that is Defibrillator Proof

Type CF Applied Part: Isolated (floating) applied part suitable for intentional external and internal application to the patient excluding direct cardiac application. The “paddles” outside the box indicate that the part is defibrillator proof.

(Medical Standard Definition:) F-Type applied part (floating/isolated) complying with the specified requirements of IEC 60601-1/UL 2601-1/CSA 601.1 Medical Standards provide a higher degree of protection against electric shock than that provided by Type B applied parts.

Type BF Applied Part

Type BF (IEC 60601-1) protection against electric shock. Isolated (floating) applied part suitable for intentional external and internal application to the patient, excluding direct cardiac application.

Type BF Equipment that is Defibrillator Proof

Type BF Applied Part that is defibrillator proof: Isolated (floating) applied part suitable for intentional external and internal application to the patient excluding direct cardiac application. “Paddles outside the box indicate the applied part is defibrillator proof.

IPX1

Atmospheric Pressure Limits

Temperature Limits

Humidity Limits

Protected against potentially harmful effects of vertically falling water drops.

Consult accompanying documents.

Caution

NOTE: Per IEC 60601-1 2nd ed, the description of this symbol is “Attention, consult ACCOMPANYING DOCUMENTS”.

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Equipment Symbols Descriptions

Mandatory Action: Follow Instructions For Use

Read and understand the operator's manual before using the device or product.

As a mandatory action sign, this symbol is identified by a blue background and white symbol.

WARNING

General warning sign.

This symbol is identified by a yellow background, black triangular band, and a black symbol.

Input Symbol

Identifies the device manufacturer and date of manufacture, if indicated.

Introduction

Date of manufacture.

Identifies the product’s catalog, or orderable part number.

Identifies the unit’s serial number.

Battery

Communication

ePort Connection

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Introduction

Equipment Symbols Descriptions

Power

Network Connection/Interface

Serial Connection/Interface

USB Connection Interface

WARNING: SHOCK HAZARD

Remove power cord from the mains source by grasping the plug. Do not pull on the cable. This may cause cable damage, which could result in loss of protective earthing or exposure to mains voltage.

Zero All

Recyclable Lithium-Ion

Recycled materials or may be recycled

Indicates Safe Working Load for the Mobile Workstand

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Chapter 2

Equipment Overview

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-1

Page 38

Equipment Overview

Serial Number Identification

Every Mac-Lab/SpecialsLab system has a unique serial number for identification. The serial

number appears on the product labels which are located (while facing the product):

 Acquisition Computer — on the front

 Review Workstation — on the front

 Centricity Cardiology INW Server — on the front

 Integrated Electronics Box (IEB) — on the back

 PDM — on the bottom

 PDM Base Station/PDM Base Station Plus — on the back

 TRAM-RAC — on the right side

 TRAM — on the back

 CardioLab II Plus Amplifier — on the back

 CO

Module — on the right side

GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC., 8200 WEST TOWER AVE., MILWAUKEE, WISCONSIN USA

Identification Tag

Item Name Description

1 Manufacture Date Date of manufacture in YYYY-MM format.

2 Part Number of Product GE Healthcare part number for product.

3 Product Code Description Identifier for type of product.

4 Serial Number and

Barcode

5 Manufacturer Information Name and address of device manufacturer.

Unique serial number for identification. Encoded as a barcode below the displayed number.

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Page 39

Typical Acquisition System Configuration

IEB

Amplifier

CIM

Bed

Generator

Catheter

Personality

Module

Mouse

Printer

Speakers

Stimulator

Real-Time

Monitor

Review Monitor

Remote

Real-Time

Monitor

3" Ceiling Conduit

3" Floor Conduit

Remote

Review

Monitor

Image

Monitor

INW

Server

CVIS

Server

Network

Switch

To Hospital Network

Keyboard

Workstation

Dashed lines indicate CardioLab/ComboLab only

Procedure Room

Control Room

IT Control Room

Monitor Boom

CPU

UPS

Vivid

Trackball

CARTO

Vivid

PDM

BASE

STATION /

PDM

BASE

STATION

PLUS

This system may consist of either Mac-Lab (hemodynamic), CardioLab (electrophysiologic) or

ComboLab (both systems).

The system may be standalone or connected to a network. Network installations include a

Centricity Cardiology INW server. In this manual, INW refers to Centricity Cardiology INW. It may

be connected to an optional CVIS server.

The system may also include a CardioLab II Plus Amplifier, also referred to as CLab II Plus.

The following block diagram shows a typical setup.

Equipment Overview

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Equipment Overview

Control Room Components

 Acquisition Computer: The Acquisition Computer provides the ability to record the patient's

real time waveform data. It uses Windows and has the following drives:

 DVD-Drive: used for installation and service of the computer.

 SD Drive: used to store backup copies of patient procedure data.

The required media for the SD Card Drive is an SDHC card with capacity of at least 16GB, and speed of at least Class 6 (Class 10 and higher is also acceptable).

 Monitors: Two monitors are standard to display Real-Time and Review windows. An optional

third monitor displays images acquired from the X-ray and ultrasound system.

 Integrated Electronics Box (IEB): The IEB provides isolated power to system components

and distributes video and communication signals to the control and procedure rooms.

 Uninterrupted Power Supply (UPS): The UPS provides emergency power to the acquisition

computer in the event of a power outage. It will sustain power to the computer for a minimum of 20 seconds. It does not power the monitors during an outage. When the UPS battery is low, it will beep. If this happens, do not attempt to replace the battery. Contact a GE Healthcare representative.

NOTE: The UPS is external to the IEB and provides uninterrupted power to the HP computer.

The monitors and other peripherals will not remain on if power is lost.

 Printer: Used to print snapshots, images and reports during or after a procedure.

 Barcode scanner (optional): Used to scan in supplies and medication used in a procedure.

 CARTO Mapping System (optional) - CardioLab or ComboLab systems only: Provides

3D electroanatomical cardiac maps to the CardioLab.

 Cardiac Stimulator (optional) - CardioLab or ComboLab systems only: Provides direct

cardiac stimulation to assist the physician during a CardioLab case.

 Vivid System Remote Trackball (optional): Provides the ability to control the GE Vivid

Ultrasound System from the control room.

 Desk (optional): Provides a workspace for control room components.

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Procedure Room Components

 Monitors: One remote monitor is standard and is software switchable between Real-Time,

Review and Image (if available) windows. A second monitor is optional.

 Remote Speakers: Provide output for ECG QRS tone and optional audible indicators in the

procedure room.

 PDM Base Station Plus: Provide power and communication to the PDM and CO2 modules.

 TRAMNet or PDM: The TRAMNet or PDM acquires invasive pressure and ECG signal data

for Mac-Lab systems. It also acquires patient vital data such as respiration rate, noninvasive blood pressure, SpO TRAMNet consists of a Remote Acquisition Case (RAC 4A) and a Transport Remote Acquisition Module (TRAM). The PDM is powered by the PDM Base Station/PDM Base Station Plus unit.

 CardioLab II Plus Amplifier - CardioLab or ComboLab systems only: The Amplifier

gathers intracardiac and surface ECG data for both the CardioLab and ComboLab systems.

 Catheter Input Modules - CardioLab or ComboLab systems only: Used for connecting

intracardiac catheters to the CardioLab II Plus Amplifier.

 RF Filter Box - CardioLab or ComboLab systems only: Filters RF noise from intracardiac

signals acquired by an ablation device.

 CO

Module (optional): The CO2 module displays the patient's respiration data on the Mac-

Lab or CardioLab System. If using TRAM, the CO PDM, the CO

 Remote Operators Terminal (RMOT) (optional): The RMOT consists of two monitors, a

module is powered by the PDM Base Station Plus.

keyboard and a mouse remotely connected to the Acquisition system to provide remote control of the Acquisition computer in the procedure room.

 Large Display Monitor (LDM) (optional): The LDM is a large widescreen flat-panel LCD

monitor used for simultaneous display of several image sources, including the Acquisition system.

 Analog Output Box (optional): Distributes ECG and blood pressure signals from the

PDM, TRAM or CardioLab Amplifier to other equipment.

 CARTO System (Patient Interface Unit) (optional) - CardioLab or ComboLab systems

only: The CARTO PIU gathers data for the CARTO system.

 Ablation Device (optional) - CardioLab or ComboLab systems only: An RF ablation

device uses radiofrequency energy to destroy abnormal electrical pathways in heart tissue. A Cryoablation device uses a coolant which flows through the catheter to freeze and destroy abnormal electrical pathways in heart tissue.

 Vivid System (optional): A digital imaging GE Ultrasound system.

 Nurse’s Review Workstation (optional): The Nurse’s Workstation is a system used in the

procedure room during a study. Provides the operator with the ability to participate in an active study and perform actions such as document administered medications and supplies consumed.

and temperature for both Mac-Lab and CardioLab systems. The

Equipment Overview

module plugs into the RAC 4A. If using

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-5

Page 42

Equipment Overview

CVIS Server

INW Server

Review

Workstation

Mac-Lab CardioLab

Hospital

Enterprise

IT Control Room Components

The INW and CVIS servers should not be used in the Patient vicinity as the servers are

Information Technology Equipment (ITE).

 Network Switch: Provides connection between network components and segments.

 Centricity Cardiology INW Server: Provides the ability to review patient data during and after

data acquisition and allows for a centralized point of data access.

 Monitor (temporary): Displays screens during server installation only. Removed after

server installation is complete.

 Keyboard (temporary): Provides an input for commands and text entries during server

installation only. Removed after server installation is complete.

 CVIS Server: Provides a central location to manage data regarding staff, supplies, inventory,

patient scheduling, patient information and statistical reports.

 Monitor (temporary): Displays screens during server installation only. Removed after

server installation is complete.

 Keyboard (temporary): Provides an input for commands and text entries during server

installation only. Removed after server installation is complete.

Network Connections

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Review Workstations

Mac-Lab/CardioLab software can run on hardware provided by GE (Review Workstation) or on

hardware provided by the hospital.

Nurse's Workstation Components

The Nurse's Workstation is a system used in the procedure room during a study.

 GE Client Workstation: Provides the operator with the ability to participate in an active study

and perform actions such as document administered medications and supplies consumed.

 Workstation Desk (optional): Provides storage and workspace for Nurse’s Workstation

components.

 Isolation Transformer: Provides isolated power for Review Workstation and monitor.

 Monitor: Used to display the Review window. One monitor is standard.

 Barcode Scanner (optional): Used to scan in supplies and medications used in a procedure.

Equipment Overview

Remote Review Workstation Components

The Remote Review Workstation is a system installed in the physician’s office or an area outside

the laboratory.

 GE Client Workstation: Used to review previously acquired procedure data and generate

reports.

 Isolation Transformer: Provides isolated power for Review Workstation and monitor.

 Monitor: Used to display the Review window. One monitor is standard.

 Printer (optional): Used to print snapshots, images and reports after a procedure.

Pre/Post Review Workstation Components

The Pre/Post Review Workstation is a Review Workstation typically located in a Holding Area for

the entry of basic patient demographics, clinical data and patient events prior to, or after, the

patient's entry into the Laboratory.

 GE Client Workstation: Used before and after the procedure to record patient information.

 DASH/Solar Monitor: Connected to the Pre/Post Workstation to acquire patient vitals during

pre or post procedure monitoring.

NOTE: The Solar and DASH monitors must only be connected to Pre/Post workstations. Do not

connect a Solar or DASH monitor to an Acquisition, Nurse's or Remote workstation.

 Monitor: Used to display the Review window. One monitor is standard.

 Isolation Transformer: Provides isolated power for the Pre/Post Workstation.

 Mobile Workstand (optional): Provides portable support for Pre/Post Workstation

components.

 Barcode Scanner (optional): Used to scan in supplies and medications used in a procedure.

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Equipment Overview

Supported Peripheral Devices

The following peripheral devices are supported for use on Mac-Lab/CardioLab/Centricity

Cardiology INW system:

 DASH: 3000/4000/5000

 Solar: 8000i and 8000M connected with a TRAM or PDM

 TRAM: 250SL, 451, 451M, 451N, 451N5, 400SL, 450SL, and 650SL

 PDM:

 2041390-058 PDM MLCL MASIMO SPO2

 2041390-059 PDM MLCL NELLCOR SPO2

 For a list of compatible PDM firmware, see the software compatibility matrix on the

Invasive Cardiology product security website:

http://www3.gehealthcare.com/en/support/New_Invasive_Cardiology_Product_Security

 Vivid: i/q

 FFR (Mac-Lab only): Radi PressureWire Aeris and Volcano SmartMap Pressure Instrument

 Ablation (CardioLab only):

 Atakr II (Model: 4803) RF (Radio frequency) ablation device

 EPT-1000 (Model: 800T) RF ablation device

 Stockert RF ablation device

 SmartAblate

 IBI 1500 (Model T6 and T12) RF ablation device

 HAT 300S RF ablation device

 CryoCath (Model: Gen3) cryo-ablation device

 JLLCABL-IT RF ablation device

 Maestro 3000

 Force device availability varies by region, please see your sales representative.

 Cardiac Stimulator (CardioLab only): MicroPace EPS 320, Bloom Stimulator

 Mapping System (CardioLab only): CARTO 3

 X-ray systems: refer to the product's DICOM conformance statement on the following GE

Healthcare website:

http://www.gehealthcare.com/usen/interoperability/dicom/products/cvinfosys_dicom.html

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System Hardware

WARNING: SHOCK HAZARD

To reduce the risk of shock and equipment damage, use safe working practices when servicing electrical equipment.

Acquisition System Components

HP z440 Computer

The Acquisition system has the following components:

 Primary Hard Drive with two partitions

 C: Application partition

 D: Data partition

Equipment Overview

 SD drive with front access (Drive E:)

NOTE: The drive used to store backups of application studies is determined by the file paths set

under System Settings in the main application menu.

 DVD drive (Drive F:)

 SD drive with internal access (Drive G:)

NOTE: The drive used for GE Service to store upgrade/migration data as well as backed up

system settings.

 Four standard expansion cards (plus optional cards)

 Matrox M9140 video board provides video out for the Real-Time (Video 1), Review (Video

2) and optional (Video 3) monitors.

 TRAMNet to Ethernet Adapter board for communication with the TRAM in the RAC 4A.

 PCI Communication board provides Amplifier Communication, Analog and Digital I/O and

Switched video (the video out from the IEB).

 Dual NIC Adapter board provides Network connection.

 Optional Matrox OrionHD board provides image capture for X-Ray or other imaging

systems.

 Serial Adapter Card provides serial interface to ablation generator.

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Equipment Overview

External Components and Connections for the HP z440

Label Part Number Description

1 2050067-002 SD Drive

2DVD Drive

3 N/A Power Switch

4 N/A LEDs, USB, Firewire and Audio connections

5 N/A Backplane I/O panel

6 N/A Board Slots

7 N/A AC Power

Not Shown 2026539-001 HP USB 2-Button Optical Mouse with Wheel

Not Shown Various Keyboard (dependent on language)

DVD Drive

SD Drive

The DVD drive is used for servicing the computer.

The SD drive contains two SD card slots: one external access slot (front of computer) for facility

personnel use and one internal access slot for use by GE service personnel.

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Equipment Overview

NOTE: The drive used to store backups of application studies is determined by the file paths set

under System Settings in the main application menu.

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Equipment Overview

HP z440 Installed Boards

Dual Port Gigabit NIC Card

 Part Number: 2089029-002

 Location: Slot 4

 Function: Network connection card.

 I/O: Two network connection jacks.

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Equipment Overview

Matrox M9140 Quad Video Board

 Part Number: 2049434-001

 Location: Slot 2

 Function: Video out for Monitor 1, Monitor 2 and Monitor 3 (optional)

 I/O: One proprietary connector. Provides four DVI/VGA output ports through a custom

connector.

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Equipment Overview

Matrox OrionHD Image Capture Board

 Part Number: 2088825-001

 Location: Slot 5

 Function: Image capture for X-Ray or other imaging systems. Used on CardioICE and

 I/O: One proprietary connector. Provides four DVI/VGA output ports through a custom

CardioImage Acquisition systems only.

connector.

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Page 51

Equipment Overview

TRAMNet to Ethernet Adapter Board

 Part Number: 2072598-001

 Location: Slot 1

 Function: Provides communication with the TRAM in the RAC 4A and converts signals from

the TRAM to the ethernet.

 I/O: Network Interface Port and 9-Pin D connector

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Equipment Overview

PCI Communication Board

 Part Number: 2014935-003

 Location: Slot 6

 Functions:

 I/O: D-Connector to IEB, Fiber Optic Jacks to the Amplifier

 Communicates with the CLab II Plus Amplifier via the fiber optic connectors

 Analog and Digital communication with the IEB via the D-Connector

 Provides the video switching signal for the Switched Video output on the IEB via the D-

Connector

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Serial Port Adapter Board

 Part Number: 2090761-001

 Location: Slot 3

 Function:

 Connection to ablation generator

 I/O: Serial cable from ablation generator

Equipment Overview

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Equipment Overview

Integrated Electronics Box (IEB)

The IEB provides power to local system components and signal pass through video and

communications. Three versions of the IEB are available to handle different line voltages: 100, 120

and 240 VAC.

The IEB consists of the following components:

 Video Multiplexer (VID MUX) board to distribute video signals from the video cards in the

Acquisition system to the monitors.

 DB Connect board to provide signal pass through for other system components.

 Isolation transformer:

 Conforms to IEC 60601-1

 2.0 kVA medical grade high-isolation transformation

 Provides either 120 VAC (for 100 and 120 VAC systems) or 240 VAC. The primary and

secondary windings are wired in parallel for 120 VAC and in series for 240 VAC.

CAUTION: CONNECTIONS

If the transformer must be disconnected for any reason, ensure the connections are correct.

 UPS (either 100, 120, or 240 VAC) and Power Distribution panel provide conditioned power to

local system components.

NOTE: The UPS is external to the IEB and provides uninterrupted power to the Acquisition

system. The monitors and other peripherials will not remain on if power is lost.

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External Components and Connections

Equipment Overview

Item Part Number Description

1 2003681-004 VID MUX Board

2 2003680-002 DB Connect Board

3 N/A Power Connections. The bottom right connector is for the Acquisition system and the

four vertical connectors on the right and left are for peripheral equipment.

4 N/A Thermal Overcurrent Circuit Breaker. This breaker protects all internal components and

5 N/A Main Power Switch. This switch controls power to all internal components and external

external devices connected to the IEB.

devices except the Acquisition system.

Both the Main Power switch on the front of the IEB and the Thermal Overload circuit breaker on

the back must be on for the system to power up.

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Equipment Overview

Video Multiplexer (VID/MUX) Board

Item Description

1 Switched video out (Video 1 or 2). This is used when the facility has only one remote monitor. To switch

monitors:

 Mac-Lab: Go to the main menu and select Windows > Physician Video.

 CardioLab: Use the dropdown box just under the main menu.

2 Video 1 (Real-Time) out to local monitor (bottom) and remote monitor (top)

3 Video 2 (Review) out to local monitor (bottom) and remote monitor (top)

4 Video 3 (CardioImage) out to local monitor (bottom) and remote monitor (top)

5 (L to R) Video 1, Video 2, Video 3 in from Acquisition system Matrox Quad Video board for Vid 1, Vid 2 and

Vid 3

The VID MUX board amplifies (±5V 1.25A) from the internal IEB DC power supply (refer to Internal

Components and Connections on page 2-23) and distributes the video signals from the HP

Computer (refer to HP z440 Video Connections on page 2-51).

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DB Connect Board

WARNING: SHOCK HAZARD

Do not connect analog input or analog output cables to patient-isolated equipment interfaces. This could compromise patient safety.

Equipment Overview

Item Description

1 Analog I/O Communication: Connects to the Acquisition system PCI Communication board.

2 Analog In: From another system (for example, Fluoro and so on)

3 Connection to the Analog Output Box

4 Analog Out (for example, Stimulator, Vivid and so on).

5 I/O TRAM (includes 16.5 VDC power)

6 Output to Acquisition system TRAMNet to Ethernet to Adapter board

Refer to the following cabling diagrams:

 Communications Connections on page 2-52

 TRAM/Amplifier Connections on page 2-53

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Equipment Overview

Power Connections

1 and 5 AC out to local equipment (6A at 120 VAC

Item Description

; 3A at 240 VAC

max

)

2 Thermal Overcurrent circuit breaker. Protects all internal components and external devices connected to

the IEB.

3 AC main power in (15A at 120 VAC

4 AC power out to UPS (2A at 120 VAC

; 7A at 240 VAC

max

; 1A at 240 VAC

max

)

max

Refer to the cabling diagram, Power Connections on page 2-50.

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Internal Components and Connections

Equipment Overview

Item Part Number Description

1 2003681-004

2003680-002

2 2013535-001 Power Supply: Provides + 5 VDC 1.25A for the VID/MUX board and +16.5 VDC for the

VID/MUX Board Assembly DB Connect (I/O) Board Assembly

RAC-4A.

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Equipment Overview

Uninterruptible Power Supply (UPS)

The UPS is designed to maintain power to the Acquisition system during a power outage for up to

20 seconds.

NOTE: The UPS is external to the IEB and provides uninterrupted power to the Acquisition

system. The monitors and other peripherials will not remain on if power is lost.

Part Number Description

2034077-002 UPS Powercom, 120V, 50/60 Hz, 1500 VA, BNT

2034078-002 UPS Powercom, 230V, 50/60 Hz, 1500 VA, BNT

2034079-002 UPS Powercom, 100V, 50/60 Hz, 1500 VA, BNT

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Page 61

Review Workstation

There are several configuration options for use of the Review Workstations in a networked system

environment.

 Nursing Workstation: A system used in the procedure room during a study.

 Remote Review Workstation: A system installed in the physician’s office or an area outside

the laboratory.

 Pre/Post Procedure Workstation: Typically located in a Holding Area for the entry of basic

patient demographics, clinical data and patient events prior to, or after, the patient's entry into the Laboratory.

NOTE: Automatic vitals logging is also available with the optional DASH and Solar monitor

interface.

NOTE: When used in a patient care area, the hardware must meet IEC60601-1. This can be

achieved through the use of a medical grade computer, separate isolation transformer or other means as determined by appropriate hospital personal.

Equipment Overview

The Review Workstation has the following components:

 Primary Hard Drive (RAID 1 configured) with four partitions:

 C: Application partition

 D: Data partition

 G: Second Hard Drive partition

 H: HP_Tools partition

NOTE: On the Review Workstation, the 32 GB Second Hard Drive partition is used to service the

system.

 One standard expansion card

 NIVIDIA NVS 310 provides video output.

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Equipment Overview

External Components and Connections for the Review Workstation

Item Part Number Description

1 N/A DVD drive

2 N/A Power button

3 N/A USB and audio connections

4 Various Keyboard (dependent on language)

5 N/A USB 2-button optical mouse with wheel

6 N/A RJ-45 port to network

7 N/A Com port for DASH/Solar connection

8 N/A Video output

9 N/A AC Power

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Page 63

Mobile Workstand

Refer to the instructions included with the mobile workstand for details on how to place the GE

hardware on an assembled GE mobile workstand (PN 2008203-001).

Equipment Overview

Item Part Number Description

1 N/A DASH Monitor

2 N/A Mouse or Barcode Scanner Location

3 N/A Keyboard Location

4 2088969-001 Review Workstation Computer

5 2004195-001 Isolation Transformer

6 2079070-002 LCD Monitor

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Equipment Overview

Monitors

The standard Acquisition system comes with two monitors and may have a third optional monitor.

The monitors include:

 A Real-Time monitor to display active patient information. It is usually located on the left.

 A Review monitor to display saved patient study information.

 An optional Image monitor (used with the CardioImage option) displays live or frozen video

A single remote monitor is standard and receives input from the switched video out (Video 1 or 2)

jack on the IEB (see External Components and Connections on page 2-19).

 To switch video for the Mac-Lab go to the main menu and select Windows > Physician

 To switch video for the CardioLab use the drop-down box just under the main menu.

images.

Video.

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Page 65

Patient Data Module (PDM)

PDM acts as an amplifier for the Mac-Lab system and is responsible for patient data acquisition. It

is connected to the PDM Base Station unit which powers the PDM and is placed in the procedure

room near the patient table. The PDM rests in a dock that can be mounted to a bed rail, a pole, or

a stand which also holds the PDM Base Station/PDM Base Station Plus.

Equipment Overview

PDM has the following patient data input features:

 Electrocardiogram (ECG): Green connector (5 or 10 leads)

 Thermal Dilution Cardiac Output (TDCO) or Temperature: Brown connector

 Invasive Blood Pressure (IBP): Red connectors

 Pulse Oximetry (SpO

 Non-Invasive Blood Pressure (NIBP): Black Connector

 Analog Out and Defib/Sync: White connector

PDM with PDM Base Station does not support CO

Base Station Plus, an optional CO

): Blue Connector

module can acquire end-tidal CO2 data.

data acquisition. When using PDM with PDM

The PDM can monitor up to four invasive blood pressures when two Y-adapter cables are used.

Plugging one Y-adapter cable into the P1/P3 connector on the PDM allows two separate invasive

blood pressures to be monitored from that connector, for a total of three pressures. Plugging a

second Y-adapter cable into the P2/P4 connector on the PDM allows two separate invasive blood

pressures to be monitored from that connector, for a total of four pressures.

NOTE: The labeling on the Y-adaptor cable (IP1 and IP2) corresponds to the first and second

pressures listed below the connector on the PDM. For example, if a Y-adaptor cable is plugged into the P1/P3 connector on the PDM, the IP1 represents P1 and the IP2 represents P3.

NOTE: The PDM waveform defibrillation recovery time is ten seconds.

Refer to Appendix E for information about the PDM battery. Refer to the Mac-Lab/CardioLab/

ComboLab/SpecialsLab Accessories Supplement (PN 2102845-001) for a list of accessories

approved for use with the PDM.

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Page 66

Equipment Overview

Ensure that the cables are compatible with the PDM, including that the SpO2 cable matches the

SpO

sensor type.

WARNING: SHOCK HAZARD

Defibrillator protection is only guaranteed when approved accessories are used. Do not use unspecified accessories.

WARNING: EXPLOSION

Do not use this equipment in the presence of flammable anesthetics, vapors or liquids.

Analog Out and Defib/Sync

The white connector on the PDM may be used to provide Analog Output or Defib/Sync signals to

external devices.

 Analog Out: This supplies either an ECG or an invasive pressure signal to another device.

Refer to Analog Output Box on page 2-46 for details.

 Defib/Sync: This provides the ECG synchronization signal for an external defibrillator,

intraaortic balloon pump or ventilator. The sync signal is generated using the currently selected ECG analog output lead. Use the Defib/Sync Interface cable (PN 2017842-001) to access this output.

An optional splitter (PN 2024565-002) may be used to provide both Analog Out and Defib/Sync

signals simultaneously.

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Page 67

PDM Base Station

12 3

The PDM Base Station powers the PDM and routes Ethernet signals between the Acquisition

system and the PDM. The PDM and Base Station are located in the procedure room near the

procedure table.

A green power light indicates the Base Station is attached to AC power and is turned on.

Equipment Overview

Item Description

1 To Acquisition System Workstation

2To PDM

3 AC power 100-240VAC 50/60Hz

PDM Base Station Plus

The PDM Base Station Plus powers and communicates with the PDM and C02 module. The PDM

and Base Station Plus are located in the procedure room near the procedure table.

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Page 68

Equipment Overview

A green power light indicates the Base Station is attached to AC power and is turned on.

Item Description

1 For future use

2To C0

module

12 3

Item Description

1To PDM

2 To Acquisition System Workstation

3 AC power 100-240VAC 50/60Hz

PDM and Base Station Mounting Options

The PDM Base Station can be mounted to a stand where the PDM is also docked.

NOTE: The green light on the front of the PDM Base Station is quite bright. It is suggested that

the PDM Base Station is installed facing away from the physician, toward the foot or the far side of the bed.

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Equipment Overview

The PDM Base Station may also rest with its feet on the floor, connected to the PDM by a longer

cable. In this setup, the PDM dock is attached to the pole/rail clamp, which clamps onto a bed rail

or pole. The pole/rail clamp is attached and detached by adjusting the clamp knob. Ensure the

knob is fully tightened when clamping to bed rails and poles.

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Equipment Overview

WARNING: TRIPPING HAZARD

Keep cables away from accessible walkways. Failure to do so may present a tripping hazard and could result in cable damage.

WARNING: FALLING EQUIPMENT

Do not place the PDM more than 147 cm (58 in) from the floor when mounting on an IV pole with a base less than 58 cm (23 in) in diameter. This may cause the IV pole to tip over.

WARNING: SHOCK HAZARD

To reduce the risk of ingress of water into the equipment, do not mount the PDM in a vertical position with the patient cables facing up or down.

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Page 71

TRAMNet

Equipment Overview

Item Description

1 TRAM Module

2 To Analog Out Box

3 To IEB TRAM Connector

The TRAMNet consists of a Remote Acquisition Case (RAC-4A) and one TRAM module. The

TRAMNet is located in the procedure room near the procedure table.

The TRAM module receives patient inputs and then transmits signal data to the IEB and other

equipment through the Analog Output Box (refer to the cabling diagrams in TRAM/Amplifier

Connections on page 2-53).

TRAM Module Inputs:

 Electrocardiogram (ECG) - green connector (5 or 10 leads)

 Thermal Dilution Cardiac Output (TDCO) - brown connector

 Invasive Blood Pressure (IBP) - 3 red connectors

 Non-Invasive Blood Pressure (NIBP) - black connector

 Pulse Oximetry (SpO

) - blue connector

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Page 72

Equipment Overview

Outputs: Analog output connector.

Refer to the documentation included with the TRAM module for additional information on

equipment and compatible accessories.

RAC 4A

The RAC 4A is the housing device for the TRAM and is mounted in the procedure room near the

procedure table. The RAC 4A can be placed on the floor or mounted to the table vertically or

horizontally and should be protected from fluids.

Refer to the documentation included with the TRAM module for additional information on

equipment and compatible accessories.

WARNING: SHOCK HAZARD

Use caution when cleaning the environment near equipment. Fluid ingress may damage devices or compromise electrical safety.

CardioLab II Plus Amplifier

The CardioLab II Plus Amplifier is designed to amplify various types of cardiac signals that are

acquired from a patient and transmit them back to the CardioLab system. These signals include 12

Lead ECG, intracardiac and pressure signals.

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Page 73

Front View

Equipment Overview

Front View 64 Channels - CardioLab II Plus Amplifier

Item Description

1 Catheter Inputs: Up to three catheter inputs will each accept a 32 pole catheter input module. Use the

CardioLab II Plus Catheter Input Modules (part number 301-00202-08) with the CardioLab II Plus Amplifier.

2 Power Indicators: The power indicator is on as long as the CardioLab II Plus Amplifier is turned on.

3 Communication Indicators: Three communication indicators show the status of the communication

between the acquisition computer and the CardioLab II Plus Amplifier.

 When the XMT indicator is on, the CardioLab II Plus Amplifier is transmitting data to the acquisition

computer. The XMT indicator should remain on as long as the power indicator is on.

 When the RCV CMD indicator is on, the CardioLab II Plus Amplifier is receiving data from the acquisition

computer. The RCV CMD indicator will turn on as long as an instruction is being received by the amplifier.

 When the RCV ERR indicator is on, the CardioLab II Plus Amplifier may not be receiving data from the

acquisition computer in a valid format or there may be a problem with the fiber optic cable.

4 Auxiliary Inputs: The auxiliary input will accept the Auxiliary Input Cable (part number 301-00205-08).

5 Stimulator Input: The stimulator input will accept a stimulator input cable. Use the 3 ft, 15 ft or 30 ft

Touchproof Stimulator Cables (part numbers, 301-00204-03, 301-00204-15, 301-00204-30, respectively) with the CardioLab II Plus Amplifier.

6 ECG Inputs: The ECG input connector will accept a 10 lead ECG input cable.

7 Pressure Inputs: Four pressure inputs will each accept a pressure transducer that is calibrated to 5uV/V/

mmHg. See the Accessory Parts List for GE Healthcare Systems Information Technologies recommended pressure transducers.

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Page 74

Equipment Overview

Front View 128 Channels - CardioLab II Plus Amplifier

Item Description

1 Catheter Inputs: Up to seven catheter inputs will each accept a 32 pole catheter input module. Use the

CardioLab II Plus Catheter Input Modules (part number 301-00202-08) with the CardioLab II Plus Amplifier.

2 Power Indicator: The power indicator is on as long as the CardioLab II Plus Amplifier is turned on.

3 Communication Indicators: Three communication indicators show the status of the communication

between the acquisition computer and the CardioLab II Plus Amplifier.

 When the XMT indicator is on, the CardioLab II Plus Amplifier is transmitting data to the acquisition

computer. The XMT indicator should remain on as long as the power indicator is on.

 When the RCV CMD indicator is on, the CardioLab II Plus Amplifier is receiving data from the acquisition

computer. The RCV CMD indicator will turn on as long as an instruction is being received by the amplifier.

 When the RCV ERR indictor is on, the CardioLab II Plus Amplifier may not be receiving data from the

acquisition computer in a valid format or there may be a problem with the fiber optic cable.

4 Auxiliary Inputs: The auxiliary input will accept the Auxiliary Input Cable (part number 301-00205-08).

5 Stimulator Inputs: The stimulator input will accept a stimulator input cable. Use the 3 ft, 15 ft or 30 ft

Touchproof Stimulator Cables (part numbers, 301-00204-03, 301-00204-15, 301-00204-30, respectively) with the CardioLab II Plus Amplifier.

6 ECG Input: The ECG input connector will accept a 10 lead ECG input cable.

7 Pressure Inputs: Four pressure inputs will each accept a pressure transducer that is calibrated to 5uV/V/

mmHg. See the Accessory Parts List for GE Healthcare Systems Information Technologies recommended pressure transducers.

2-38 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 75

Back View of Amplifier – Generic

Equipment Overview

Back View - CardioLab II Plus Amplifier

Item Description

1 FDDI Connection to Computer: This connector will accept a FDDI type fiber optic cable. The fiber optic

cable allows for two-way communication between the amplifier and the CardioLab system.

2 Power Input: The GE-supplied power cord connects to the Power Input.

3 Equipotentiality Terminal: The Equipotentiality Terminal is connected to earth ground

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-39

Page 76

Equipment Overview

CardioLab II Plus Catheter Input Module

The equivalent to the Stimulus Inputs 1-4 on the Stimulator Input Cable are labeled on the

CardioLab II Plus Amplifier as Stimulus Inputs A1, A2, B1 and B2.

The four stimulus inputs on the Stimulator Input Cable connect to the stimulator.

Each Catheter Input Module is broken down into two groups of 16 poles each. For example, Block

A is broken into A (1-16) and A (17-32).

Each pacing channel, requires one positive and one negative pole. In order to maximize the

number of pacing channels, only one positive and one negative designation should be made for

each group.

For detailed instructions on how to designate pacing channels and enable pacing for particular

sites, refer to the on-line help in the software application.

2-40 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 77

Equipotential Grounding Box

The Equipotential Grounding Box could be used to ground patient connected equipment when an

equipotential connector on the patient table either does not exist or does not reach the device to

be connected.

How to Connect Equipotential Grounding Box

Connect the desired length equipotential cable to the equipotential connector on the back of the

amp as shown below:

Equipment Overview

Connect the other end of the cable to the equipotential connector on the patient table. If the

equipotential connector on the table is in use, use the equipotential junction box to allow for the

connection of multiple cables to the table as shown below:

All of the patient connected equipment may be connected to the table using the junction box.

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-41

Page 78

Equipment Overview

Accessory Parts List

Accessories for use with the CardioLab II Plus Amplifier are listed in the following table.

Input Type Accessories

ECG Conmed ECG Input Cable - 10 ft, AHA, 2003419-001

Conmed ECG Input Cable - 15 ft, AHA, 2003420-001

Conmed Leadwires - 3 ft, AHA, 2003421-001

Conmed Leadwires - 3 ft, IEC, 2003422-001

Conmed Leadwires - 3 ft, AHA, radiotranslucent, 2003423-001

Conmed Leadwires - 6 ft, AHA, 2003425-001

Conmed Leadwires - 6 ft, AHA, radiotranslucent, 2003424-001

Conmed Leadwires - 6 ft, IEC, radiotranslucent, 2003426-001

Invasive Blood Pressure*

Cable: Fogg Systems 0253-2256

Transducer: Medex NOVATRANS II MX860

Cable: Fogg Systems 0310-2256

Transducer: Merit Med Systems MERITRANS 100 or 210

Cable: Fogg Systems 0333-2256

Transducer: Medex TranStar MX950

Cable: Fogg Systems 0386-2256

Transducer: Medex LogiCal MX960

Cable: Fogg Systems 0389-2256

Transducer: BD DTX Plus

Cable: Fogg Systems 0391-2256

Transducer: BD P23XL-1 (684000)

Cable: Fogg Systems 0395-2256

Transducer: Edwards Lifesciences TruWave PX-600

Cable: Fogg Systems 0408-2256

Transducer: ICU medical TRANSPAC IV

Cable: Fogg Systems 0431-2256

Transducer: Namic PERCEPTOR Manifold [w/Integral Transducer]

Cable: Fogg Systems 0432-2256

Transducer: Namic PERCEPTOR DT

Intracardiac ECG Catheter Input Module, 301-00202-08

Auxiliary Input Cable, 301-00205-08

2-42 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 79

Input Type Accessories

Stimulator Stimulator Input Cable - 3 ft, 301-00204-03

Stimulator Input Cable - 15 ft, 301-00204-15

Stimulator Input Cable - 30 ft, 301-00204-30

Ablation Recording Stim Extender Cable - 3 ft, 2083472-001

*IBP accessories not sold by GE Healthcare. Transducers are 5uV/V/mmHg.

NOTE: The amplifier waveform defibrillation recovery time is five seconds.

WARNING: SHOCK HAZARD

The CardioLab II Plus amplifier defibrillation protection is only guaranteed when approved accessories are used. Do not use unspecified accessories.

Equipment Overview

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-43

Page 80

Equipment Overview

CARTO System (Patient Interface Unit)

Item Description

1 CARTO 3 PIU Output to Amplifier

NOTE: For specific information related to the operation, troubleshooting, or repair of the CARTO

System, refer to the OEM documentation. For information about the CardioLab/CARTO System interface, refer to the CardioLab Operator manual.

2-44 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 81

Equipment Overview

The CARTO System acquires and displays electroanatomical 3D images of heart chambers. This

information is displayed on the CARTO System and can be exported into the CardioLab

application.

Two connections are required: one from the CARTO System Patient Interface Unit to the

CardioLab II Plus Amplifier and another from the CARTO System computer to the Acquisition

system. Refer to the cabling diagram in CARTO 3 System Connections on page 2-62 for specific

information.

To quickly view the status of the interface, check the CARTO System icon at the bottom-right of the

Real-Time window (a heart against a grid). The color changes, depending on the system state:

 Gray: Disconnected

 Blue: Standby

 Green: Passive Interface

 Yellow: Active Interface

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-45

Page 82

Equipment Overview

Analog Output Box

WARNING: SHOCK HAZARD

Do not connect analog input or analog output cables to patient-isolated equipment interfaces. This could compromise patient safety.

Item Description

1 Input from TRAMNet or PDM

2 Input from Amplifier through the IEB

The analog output box distributes heart rate and blood pressure signals to multiple outputs (refer

to the connection diagrams in TRAM/Amplifier Connections on page 2-53 and PDM/Amplifier

Connections on page 2-54). This may be done to synch auxiliary equipment or display the

information on a scope or other device.

Patient information comes from either the TRAMNet/PDM or the Amplifier (through the IEB) and is

output through the output jacks on the top of the box:

 Channels 2-4 and 13-16 are switchable between the TRAMNet (Mac-Lab) and CardioLab II

Plus Amplifier (CardioLab).

 The remaining channels are used exclusively by CardioLab.

 Channels 1-12 may be distributed to up to 4 other devices using the selector switch.

 Channel 2 is used by the PDM for ECG and Channel 13 is used by the PDM for invasive blood

pressure.

2-46 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 83

Network Components

 Centricity Cardiology INW Server provides

 Network repository for patient studies

 Acquisition system and Review Workstation access to patient studies

 CVIS Server provides

 Central list management for staff, supplies and so on.

 Patient scheduling

 Patient information

 Inventory Management

 Statistical Reports

Centricity Cardiology INW G9 Server

The G9 server has the following specifications:

 Processor: 2.4-GHz Intel Xeon E5-2620 v3

 Separate C: and D: drives (see the following chart):

 The C: drive is RAID 1 (two 300GB drives)

 The D: drive is RAID 6 (six 1.2TB drives)

Equipment Overview

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-47

Page 84

Equipment Overview

12 3

Item Description

1 CD/DVD Drive

2 Power Switch, USB Connectors

3 Hard Drives

2-48 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 85

Cabling and Connections

z440 Computer

I/O Backplane

WARNING: SHOCK HAZARD

To reduce the risk of shock and equipment damage, use safe working practices when servicing electrical equipment.

HP z440 Computer I/O Backplane Connections

Equipment Overview

Item Part Number Description

1 N/A PS2 Connection for Keyboard

2 N/A USB Barcode Scanner Cable

3 HP 237241-001 USB Port for Mouse

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-49

4 N/A RJ-45 Port to Network

5 N/A To Speakers

6 2025965-002 USB Port for Printer (cable to use depends on the printer)

Page 86

Equipment Overview

HP z440

Computer

3 3

IEB

UPS

Power Connections

Item Part Number Description Length

4 2003927-001 AC power to UPS 8 ft

700775-002 700774-001

405535-013

80274-006

2003927-001

403689-010

120 VAC main power in 230 VAC main power in

AC power to Acquisition CPU (100V) AC power to Acquisition CPU (120V) AC power to HP Acquisition (230V)

AC to Local Equipment — Monitors, Printers, speakers and external Blu-Ray Drives AC to Remote Monitors

CAUTION: SYSTEM FAILURE

To ensure an adequate system power supply, GE Healthcare recommends using a dedicated circuit to power the IEB.

8 ft

6 ft 6 ft 8 ft

8 ft

100 ft

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Page 87

HP z440 Video Connections

HP z440

Computer

Analog IEB

Equipment Overview

Item Part Number Description Length

1 2003928-001 Real-Time display (Video 1) in to IEB 5 ft

2 2003928-001 Review display (Video 2) in to IEB 5 ft

3 2003928-001 Cardio Image display (Video 3) in to IEB 5 ft

4 2003928-001

2081540-001

5 2003928-001

2081540-001

6 2003928-001

7 2003442-003 Out to remote monitor (switched Video 1 or Video 2) 100 ft

8 2003442-003 Out to optional remote monitors (Video 1, 2, or 3) 100 ft

9a 2018060-002 Image capture. The DVI to 5-BNC female connector cable plugs into DVI

9b 2003411-002 BNC Cable to optional imaging system 50 ft

10 N/A Matrox Quad Video Adapter Cable (Included with Video Board)

2081540-001

Out to Local Cardio Image Monitor (Video 3) 5 ft

Out to Local Review Monitor (Video 2) 5 ft

Out to Local Real-Time monitor (Video 1) 5 ft

connector #3 on the Matrox KX-20 Quad video adapter cable. Only one BNC connection is used to connect to the image input from another system (9b)

6 ft

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-51

Page 88

Equipment Overview

HP z440

Acquisition System

IEB

Communications Connections

Item Part Number Description Length

1 418335-002 Network Connection 10 ft

2 2018835-001

2003408-002 2042981-001 2035570-001 2042214-001

3 2003587-002 PCI Communications (DB-44) 2.5 ft

4 2003410-001 BNC coax. Analog In (from Fluoro and so on) 30 ft

5 2003410-001 Analog Out (typically to Stimulator) 30 ft

RF Ablation Device Interface. HP z440 Acquisition system shown.

Serial Cable Optical Isolator Serial Cable for CryoCath Interface Serial Cable for RF Ablation Interface

N/A

50 ft

N/A 2 m

6 ft

2-52 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 89

TRAM/Amplifier Connections

Acquisition

System

Amplifier

TRAM-RAC

Analog

Output Box

IEB

Patient

Data

Patient

Data

Analog

Data

WARNING: SHOCK HAZARD

Do not connect analog input or analog output cables to patient-isolated equipment interfaces. This could compromise patient safety.

Equipment Overview

Item Part Number Description Length

1 * 2011129-001 TRAMNet to ethernet cable 1 ft

2 * 2016133-001 Acquisition system/IEB TRAMNet cable 3 ft

3a 417335-xxx Adapter cable to TRAM. Part number varies by length ordered (-001 to -007) Varies

3b * 2016134-001 15-pin to 9-pin adapter cable 1 ft

* These cables are contained in TRAMNet Cabling Kit (PN 2018683-001)

4 417335-002 TRAM-RAC to Analog Output Box cable 51 ft

5 2007579-001 IEB to Analog Output Box cable 15 ft

6 2003434-001 Amplifier to Acquisition system fiber optic cable 75 ft

417335-003 TRAM-RAC to Analog Output Box cable 70 ft

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-53

Page 90

Equipment Overview

Acquisition

System

Amplifier

PDM

PDM Base Station /

PDM Base Station Plus

Analog

Output Box

IEB

Patient

Data

Patient

Data

Analog

Data

PDM/Amplifier Connections

WARNING: SHOCK HAZARD

Do not connect analog input or analog output cables to patient-isolated equipment interfaces. This could compromise patient safety.

Item Part Number Description Length

2-54 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

1 418335-008 Ethernet cable from PDM Base Station to Acquisition System 100 ft

2 2062755-001 CABLE, PDM TO ANOUT BOX 15 ft

3 2007579-001 IEB to Analog Output Box cable 15 ft

4 2003434-001 Amplifier to Acquisition system fiber optic cable 75 ft

5 2017098-001 ePort PDM to Host 5 ft

2062755-002 CABLE, PDM TO ANOUT BOX 50 ft

2062755-003 CABLE, PDM TO ANOUT BOX 75 ft

2062755-004 CABLE, PDM TO ANOUT BOX 100 ft

2017098-003 ePort PDM to Host 15 ft

2017098-009 ePort PDM to Host 12.5 in

2017098-005 ePort PDM to Host 25 ft

2017098-007 ePort PDM to Host 45 ft

Page 91

PDM Base Station Plus/CO2 Connections

Typical Setup (with Capnostat 5 Mainstream CO2 Sensor)

Equipment Overview

Item Part Number Description Length

1 2077867-001 PDM BASE STATION PLUS N/A

2 2092608-001 CAPNOSTAT 5 MAINSTREAM CO2 SENSOR 10 ft

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-55

Page 92

Equipment Overview

Typical Setup (with LoFlo Sidestream CO2 Module)

Item Part Number Description Length

1 2077867-001 PDM BASE STATION PLUS N/A

2 2089969-001 CABLE CO2 EXTENDER 4FT (OPTIONAL) 4 ft

3 2092609-001 C5 LOFLO SIDESTREAM CO2 MODULE 2 ft

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Page 93

Amplifier/Stimulator Connections

IEB

Acquisition

MicroPace Stimulator

MicroPace

CPU

Amplifier

Generator

Catheter

Connection

Box

External

ECG

Auxiliary Reference

Catheter

Input

Module

Personality

Module

Typical Setup (with MicroPace)

Equipment Overview

Item Part Number Description Length

1 2003411-002 BNC Cable. Connects back of MicroPace (ECG 1 Input) to back of IEB

50 ft

(Analog Out 1).

2 N/A Large Cable with D-Connectors. Connects back of MicroPace (Auxiliary

N/A

Port) to side of Catheter Connection Box.

3 N/A Small Cable. Connects front of MicroPace (Green Connection Port or in

N/A

emergencies Red Connection Port) to side of Catheter Connection Box.

4 301-00204-03

301-00204-15 301-00204-30

Red or Black leads connect to front of Catheter Connection Box to Amplifier Stimulator Input.

3 ft 15 ft 30 ft

5 2003434-001 Fiber Optic Cable 75 ft

6 2003587-002 DB44 Connect Cable 2.5 ft

7 2003408-002 Serial Cable 50 ft

8 301-00202-08 Catheter Input Module 8 ft

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Page 94

Equipment Overview

Typical Setup (with Bloom)

Personality

Module

Generator

Acquisition

IEB

Bloom

Catheter

Input

Module

Catheter

Connection

Box

Amplifier

External

ECG

Auxiliary Reference

Item Part Number Description Length

1 2003410-001 BNC Cable. Connects Bloom to back of IEB 30 ft

2 N/A Large Cable with Square Connectors. Connects back of Bloom to back of

Patient Isolation Box.

3 N/A Small Cable. Connects front of Patient Isolation Box to side of Catheter

Connection Box.

4 301-00204-03

301-00204-15

Red or Black leads connect to front of Catheter Connection Box to Amplifier Stimulator Input.

301-00204-30

5 2003434-001 Fiber Optic Cable 75 ft

6 2003587-002 DB44 Connect Cable 2.5 ft

7 2003408-002 Serial Cable 50 ft

8 301-00202-08 Catheter Input Module 8 ft

Battery Battery

Patient

Isolation

Box

N/A

3 ft 15 ft 30 ft

2-58 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

Page 95

Equipment Setup

Item Part Number Description

C and

D N/A Patient Isolation Box. Rear connection to Bloom (C1) via large cable with square

E N/A Catheter Connection Box. Side connection to the Patient Isolation Box (D) front

F 2088700-002

Equipment Overview

N/A Bloom (This is a typical example. Specific equipment may vary by location). Connects to

the IEB (not shown) via the External Input BNC jack on the back (C1) and the Patient Isolation Box (D) via a large cable with square connectors. (See next section for detail.)

connectors. Front connection to Catheter Connection Box (E). Front panel provides access to internal batteries.

connector. Red and Black leads connect from the front to the Amplifier (F) Stim Input.

Amplifier connected to

2088700-004

G 301-00202-08 Catheter Input Module. Catheter leads (not shown) plug into the block end. Connector on

1 N/A Bloom connection to IEB (BNC cable not shown).

2 N/A Bloom connection to Patient Isolation Box.

3 N/A Patient Isolation Box to Catheter Input Module Cable.

4 301-00204-03 Catheter Connection Box to Amplifier Cable.

5 2003425-001 External ECG Connections. Colored leads connect to patient. Connector on other end

6 301-00205-08 Auxiliary Reference Cable. Plugs into the Amplifier (4) Auxiliary Input.

7 2003420-001 ECG Trunk Cable.

 (1) External ECG connection

 (2) Catheter Input Module

 (3) Auxiliary Reference Cable

 (4) Catheter Connection Box

other end plugs into the Amplifier (4) Cardiac Input (Labeled A, B, C and so on).

connects into the Amplifier (4) ECG Input.

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Page 96

Equipment Overview

Bloom (Connection Detail)

Item Description

1 External Input: BNC connection to the IEB (cable not shown).

2 J20: Connection to Patient Isolation Box (large square connector).

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Page 97

Audio

Local

Left

Speaker

Local Right

Speaker

Remote

Left

Speaker

Remote

Right

Speaker

IEB

to 60601-1

Certified

Power

Supply

z440

Equipment Overview

Item Part Number Description

1 2018218-001 Y-connector (Connects to green jack on HP. One side to local speakers, the other to remote speakers.)

2 2018219-001 Audio Isolator

3 2078970-001 Speaker Set

4 2078970-001 Speaker Power Supply (included with speakers)

5 2003927-001

6 2011108-002 Speaker cable (50 ft)

2003625-001

IEC (m) to IEC (f) Power Cord (8 ft)

NEMA to IEC Converter Cable (1 ft)

WARNING SHOCK HAZARD — Remote speakers must be powered by a 60601-1 certified power supply.

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Page 98

Equipment Overview

CARTO 3 System Connections

The CARTO 3 System may be connected in one of two ways:

 Configuration 1 (refer to the following figure) to acquire:

 HIS, RVA and HRA signals with the Catheter Input Module.

 Surface ECG via the CARTO 3 system using the ECG connectivity cable.

NOTE: Not all CARTO 3 System equipment or connections are shown. Refer to the CARTO 3

System Installation Manual for additional information.

Item Part Number Description

1 301-00202-08 Catheter Input Module

2 2088700-002 or

2088700-004

3 N/A ECG Connectivity Cable (Biosense Webster CA-5400-19)

4N/ACARTO 3 PIU

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CardioLab II Plus Amplifier

Page 99

Equipment Overview

 Configuration 2 (refer to the following figure) to acquire:

 HIS, RVA and HRA signals, Navistar Cath (mapping), Coronary Sinus, or other signals via

the CARTO 3 system using the IECG connectivity cable.

 Surface ECG via the CARTO 3 system using the ECG connectivity cable.

NOTE: The CardioLab II Plus Amplifier remains connected to all body surface leads even if the

CARTO 3 PIU is turned off.

NOTE: Not all CARTO 3 System equipment or connections are shown. Refer to the CARTO 3

System Installation Manual for additional information.

Item Part Number Description

1 N/A IECG Connectivity Cable (Biosense Webster CA-5400-21)

2 2088700-002

or 2088700-004

3 301-00202-08 Catheter Input Module

4 N/A ECG Connectivity Cable (Biosense Webster CA-5400-19)

5 N/A Stimulation Cables, 3m (Biosense Webster J-B-PACINT-AUX / CA-4041-03)

6 N/A CARTO 3 PIU Front

7 N/A CARTO 3 PIU Back

CardioLab II Plus Amplifier

2088535-010F EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2-63

Page 100

Equipment Overview

Acquisition

System

CARTO System

Computer

Item Manufacturer Part Number Description

1 GE 2018217-001 CAT5 Crossover Cable (25 ft).

2-64 Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual 2088535-010F EN

GE Mac-Lab_CardioLab_Centricity Cardiology INW Service Manual_SM_2088535-010_F Centricity Cardiology INW Service Manual Software Version 6.9.6 R2 2088535-010F EN

Specifications and Main Features

Frequently Asked Questions

User Manual

Introduction

Manual Information

Purpose

Product References

Printed Copies

Intended Audience

Operators

System Administrator

Field Service Engineer

Indications for Use

Types Of Systems

Mac-Lab System

CardioLab System

ComboLab System

SpecialsLab System

Compliance

Classification

Conventions

Illustrations and Names

Related Documents

Safety Information

Definitions

General

Applicable Messages

Responsibility of the Manufacturer

Responsibility of the User

General

Anti-Virus Software

Product Vulnerability and Security Patches

Preventative Maintenance

Service

Equipment Symbols

Equipment Overview

Serial Number Identification

Typical Acquisition System Configuration

Control Room Components

Procedure Room Components

IT Control Room Components

Network Connections

Review Workstations

Nurse's Workstation Components

Remote Review Workstation Components

Pre/Post Review Workstation Components

Supported Peripheral Devices

System Hardware

Acquisition System Components

HP z440 Computer

External Components and Connections for the HP z440

DVD Drive

SD Drive

HP z440 Installed Boards

Dual Port Gigabit NIC Card

Matrox M9140 Quad Video Board

Matrox OrionHD Image Capture Board

TRAMNet to Ethernet Adapter Board

PCI Communication Board

Serial Port Adapter Board

Integrated Electronics Box (IEB)

External Components and Connections

Video Multiplexer (VID/MUX) Board

DB Connect Board

Power Connections

Internal Components and Connections

Uninterruptible Power Supply (UPS)

Review Workstation

External Components and Connections for the Review Workstation

Mobile Workstand

Monitors

Patient Data Module (PDM)

Analog Out and Defib/Sync

PDM Base Station

PDM Base Station Plus

PDM and Base Station Mounting Options

TRAMNet

RAC 4A

CardioLab II Plus Amplifier