GE Mac-Lab_CardioLab_Centricity Cardiology INW Service Manual_SM_2097992-010_D ZONARE z.onepro Ultrasound System (Including Special Procedures interface option) Instructions for Use
The information in this manual only applies to Mac-Lab/CardioLab/Centricity Cardiology INW software version
6.9.6 R3. It does not apply to earlier software versions. Due to continuing product innovation, specifications in this
manual are subject to change without notice.
and Vivid are all trademarks of General Electric 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.
RevisionDateComment
A10 August 2016Internal release.
B31 May 2017Initial public release.
C4 December 2017Added Safe Working Load symbol to the Equipment Symbols table in Chapter 1.
Updated PDM battery warning and recycling information.
Added supported PDM peripheral devices.
Updated z440 replacement parts for fans, the power supply, and the SD reader drive and
cable.
Removed PN 2006323-001 CABLE POWER, IEC C19 TO UNTERMINATED, from the IEB
Replacement Parts List in Chapter 6.
D30 November 2018Updated for IEC/EN 60601-1-2 4th ed.
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xMac-Lab/CardioLab/Centricity Cardiology INW Service Manual2097992-010D 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 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 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
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
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 Field Service Engineer. Please refer system problems not covered in this manual to GE
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
CO
(EtCO2), temperature, hemodynamic measures (for example, valve gradients and areas,
2
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,
2
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
2
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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).
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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
IEBClass IN/A
CardioLab II Plus Amplifier:
Class I
CF Defib Proof ECG, IBP, IC ECG, Auxiliary
PDM Base StationClass IN/A
PDM Base Station PlusClass IBF
PDM
ECG, IBP, SpO
NBP
, Temp, CO
2
Class I
CF Defib Proof
BF Defib Proof
TRAM-RACClass IN/A
TRAM module:
ECG, IBP, SpO
NBP
, Temp, CO
2
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 SuitableContinuous
Capnostat Mainstream CO
CapnoFlex CO
module
2
PDM Base Station Plus LoFlo Sidestream CO
module
PDM Base Station Plus CAPNOSTAT 5
Mainstream CO
sensor
2
module
2
N/A BF
N/A BF
2
N/A BF
N/A BF
Vivid Remote TrackballN/AN/A
Ordinary
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Introduction
Conventions
The following conventions are used throughout this manual.
BoldIndicates keys on the keyboard, text to be entered or hardware items such as buttons or switches
on the equipment.
ItalicsIndicates 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
EnterPress 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.
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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 gasses (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 gasses.
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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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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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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Responsibility of the Manufacturer
GE 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.
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.
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 2097992-004) 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.
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 2097992-004) 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 service representative.
Refer equipment servicing to GE 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 or to one of their authorized
agents.
Equipment Symbols
Equipment SymbolsDescriptions
RX OnlyCAUTION: 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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Equipment SymbolsDescriptions
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:
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 SymbolsDescriptions
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
(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.
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 SymbolsDescriptions
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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Page 34
Introduction
Equipment SymbolsDescriptions
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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Page 35
Chapter 2
Equipment Overview
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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
2
2
1
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC., 8200 WEST TOWER AVE., MILWAUKEE, WISCONSIN USA
Identification Tag
ItemNameDescription
1Manufacture DateDate of manufacture in YYYY-MM format.
2Part Number of ProductGE part number for product.
3Product Code DescriptionIdentifier for type of product.
4Serial Number and
Barcode
5Manufacturer InformationName and address of device manufacturer.
Unique serial number for identification.
Encoded as a barcode below the displayed number.
3
4
5
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Page 37
Typical Acquisition System Configuration
IEB
Amplifier
CIM
Bed
RF
Generator
Catheter
Personality
Module
Mouse
Printer
Speakers
Stimulator
Real-Time
Monitor
Review
Monitor
Remote
Real-Time
Monitor
3" Ceiling Conduit
3" Floor 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 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-
2
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.
2
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
2
Equipment Overview
module plugs into the RAC 4A. If using
2
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Page 40
Equipment Overview
CVIS Server
INW Server
Review
Workstation
Mac-Lab CardioLab
Hospital
Enterprise
OR
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.
CARESCAPE/Dash/Solar Monitor: Connected to the Pre/Post Workstation to acquire patient
vitals during pre or post procedure monitoring.
NOTE: The CARESCAPE, Dash, and Solar monitors must only be connected to Pre/Post
workstations. Do not connect a CARESCAPE, Dash, or Solar 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:
CARESCAPE: B650 and B450
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
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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 (Optional) 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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Page 44
Equipment Overview
2
3
4
5
7
6
1
External Components and Connections for the HP z440
LabelPart NumberDescription
12050067-002SD Drive
2DVD Drive
3N/APower Switch
4N/ALEDs, USB, Firewire and Audio connections
5N/ABackplane I/O panel
6N/ABoard Slots
7N/AAC Power
Not Shown2026539-001HP USB 2-Button Optical Mouse with Wheel
Not ShownVariousKeyboard (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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Page 46
Equipment Overview
1
2
3
4
5
6
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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Page 47
Equipment Overview
1
2
3
4
5
6
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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Page 48
Equipment Overview
1
2
3
4
5
6
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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Equipment Overview
TRAMNet to Ethernet Adapter Board — PCI-E (optional)
1
2
3
4
5
6
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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Page 50
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
1
2
3
4
5
6
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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Page 51
Serial Port Adapter Board
1
2
3
4
5
6
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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Page 52
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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Page 53
External Components and Connections
Equipment Overview
ItemPart NumberDescription
12003681-004VID MUX Board
22003680-002DB Connect Board
3N/APower Connections. The bottom right connector is for the Acquisition system and the
four vertical connectors on the right and left are for peripheral equipment.
4N/AThermal Overcurrent Circuit Breaker. This breaker protects all internal components and
5N/AMain 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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Page 54
Equipment Overview
Video Multiplexer (VID/MUX) Board
ItemDescription
1Switched 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.
2Video 1 (Real-Time) out to local monitor (bottom) and remote monitor (top)
3Video 2 (Review) out to local monitor (bottom) and remote monitor (top)
4Video 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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Page 55
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
ItemDescription
1Analog I/O Communication: Connects to the Acquisition system PCI Communication board.
2Analog In: From another system (for example, Fluoro and so on)
3Connection to the Analog Output Box
4Analog Out (for example, Stimulator, Vivid and so on).
5I/O TRAM (includes 16.5 VDC power)
6Output 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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Page 56
Equipment Overview
Power Connections
1 and 5AC out to local equipment (6A at 120 VAC
ItemDescription
; 3A at 240 VAC
max
max
)
2Thermal Overcurrent circuit breaker. Protects all internal components and external devices connected to
the IEB.
3AC main power in (15A at 120 VAC
4AC power out to UPS (2A at 120 VAC
; 7A at 240 VAC
max
; 1A at 240 VAC
max
max
)
max
).
Refer to the cabling diagram, Power Connections on page 2-50.
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Page 57
Internal Components and Connections
Equipment Overview
ItemPart NumberDescription
12003681-004
2003680-002
22013535-001Power 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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Page 58
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 NumberDescription
2034077-002UPS Powercom, 120V, 50/60 Hz, 1500 VA, BNT
2034078-002UPS Powercom, 230V, 50/60 Hz, 1500 VA, BNT
2034079-002UPS Powercom, 100V, 50/60 Hz, 1500 VA, BNT
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Page 59
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 CARESCAPE, 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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Page 60
Equipment Overview
1
2
3
4
7
8
5
9
6
External Components and Connections for the Review Workstation
ItemPart NumberDescription
1N/ADVD drive
2N/APower button
3N/AUSB and audio connections
4VariousKeyboard (dependent on language)
5N/AUSB 2-button optical mouse with wheel
6N/ARJ-45 port to network
7N/ACom port for CARESCAPE/Dash/Solar connection
8N/AVideo output
9N/AAC Power
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Page 61
Mobile Workstand
4
1
5
6
2
3
2
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
ItemPart NumberDescription
1N/ACarescape B450 or Dash Monitor
2N/AMouse or Barcode Scanner Location
3N/AKeyboard Location
42099200-001Review Workstation Computer
CAUTION:HARDWARE INCOMPATIBILITY
The Virtual Review cannot be used with the Mobile
52004195-001Isolation Transformer
62079070-002LCD Monitor
Workstand.
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Page 62
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 63
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
2
module can acquire end-tidal CO2 data.
2
data acquisition. When using PDM with PDM
2
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. Refer to the documentation included with the PDM module for
additional information.
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Page 64
Equipment Overview
Ensure that the cables are compatible with the PDM, including that the SpO2 cable matches the
SpO
sensor type.
2
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 65
PDM Base Station
123
1
2
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
ItemDescription
1To Acquisition System Workstation
2To PDM
3AC 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.
2097992-010D EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2-31
Page 66
Equipment Overview
A green power light indicates the Base Station is attached to AC power and is turned on.
ItemDescription
1For future use
2To C0
module
2
123
ItemDescription
1To PDM
2To Acquisition System Workstation
3AC 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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Page 68
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 69
TRAMNet
Equipment Overview
ItemDescription
1TRAM Module
2To Analog Out Box
3To 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
2
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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 71
Front View
Equipment Overview
Front View 64 Channels - CardioLab II Plus Amplifier
ItemDescription
1Catheter 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.
2Power Indicators: The power indicator is on as long as the CardioLab II Plus Amplifier is turned on.
3Communication 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.
4Auxiliary Inputs: The auxiliary input will accept the Auxiliary Input Cable (part number 301-00205-08).
5Stimulator 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.
6ECG Inputs: The ECG input connector will accept a 10 lead ECG input cable.
7Pressure Inputs: Four pressure inputs will each accept a pressure transducer that is calibrated to 5uV/V/
mmHg. See the Accessory Parts List for GE Medical Systems Information Technologies recommended
pressure transducers.
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Page 72
Equipment Overview
1
7
6
4
5
2
Front View 128 Channels - CardioLab II Plus Amplifier
ItemDescription
1Catheter 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.
2Power Indicator: The power indicator is on as long as the CardioLab II Plus Amplifier is turned on.
3Communication 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.
4Auxiliary Inputs: The auxiliary input will accept the Auxiliary Input Cable (part number 301-00205-08).
5Stimulator 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.
6ECG Input: The ECG input connector will accept a 10 lead ECG input cable.
7Pressure Inputs: Four pressure inputs will each accept a pressure transducer that is calibrated to 5uV/V/
mmHg. See the Accessory Parts List for GE Medical Systems Information Technologies recommended
pressure transducers.
3
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Page 73
Back View of Amplifier – Generic
Equipment Overview
Back View - CardioLab II Plus Amplifier
ItemDescription
1FDDI 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.
2Power Input: The GE-supplied power cord connects to the Power Input.
3Equipotentiality Terminal: The Equipotentiality Terminal is connected to earth ground
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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.
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Page 75
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.
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Equipment Overview
Accessory Parts List
Accessories for use with the CardioLab II Plus Amplifier are listed in the following table.
*IBP accessories not sold by GE. 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
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Page 78
Equipment Overview
CARTO System (Patient Interface Unit)
1
ItemDescription
1CARTO 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.
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Page 79
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
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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.
ItemDescription
1Input from TRAMNet or PDM
2Input 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.
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Page 81
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
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Page 82
Equipment Overview
123
ItemDescription
1CD/DVD Drive
2Power Switch, USB Connectors
3Hard Drives
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Page 83
Cabling and Connections
z440 Computer
I/O Backplane
1
2
3
4
6
5
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
ItemPart NumberDescription
1N/APS2 Connection for Keyboard
2N/AUSB Barcode Scanner Cable
3HP 237241-001USB Port for Mouse
2097992-010D EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2-49
4N/ARJ-45 Port to Network
5N/ATo Speakers
62025965-002USB Port for Printer (cable to use depends on the printer)
Page 84
Equipment Overview
HP z440
Computer
33
2
1
IEB
4
UPS
Power Connections
ItemPart NumberDescriptionLength
1
2
3
42003927-001AC power to UPS8 ft-
# Voltage rating of cables passing through conduits only
700775-002
700774-001
405535-013
80274-006
2003927-001
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
8 ft-
6 ft
6 ft
8 ft
8 ft
100 ft
CAUTION: SYSTEM FAILURE
To ensure an adequate system power supply, GE recommends using a
dedicated circuit to power the IEB.
Voltage
Rating
#
-
-
-
-
300V
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Page 85
HP z440 Video Connections
7
6
4
5
8
9b
9a
2
HP z440
Computer
Analog IEB
3
1
10
10
Equipment Overview
ItemPart NumberDescriptionLength
12003928-001Real-Time display (Video 1) in to IEB5 ft-
22003928-001Review display (Video 2) in to IEB5 ft-
32003928-001Cardio Image display (Video 3) in to IEB5 ft-
42003928-001
52003928-001
62003928-001
72003442-003Out to remote monitor (switched Video 1 or Video 2)100 ft30V
82003442-003Out to optional remote monitors (Video 1, 2, or 3)100 ft30V
9a2018060-002Image capture. The DVI to 5-BNC female connector cable plugs
9b
10N/AMatrox Quad Video Adapter Cable (Included with Video Board)
# Voltage rating of cables passing through conduits only
or
2081540-001
or
2081540-001
or
2081540-001
2003411-002
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
into DVI 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)
#
BNC Cable to optional imaging system50 ft300V
or
6 ft
or
6 ft
or
6 ft
Voltage
Rating
#
-
-
-
-
-
-
-
-
-
-
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Page 86
Equipment Overview
HP z440
Acquisition System
IEB
3
4
2
1
5
Communications Connections
ItemPart NumberDescriptionLength
1418335-002Network Connection10 ft-
2
2003408-002
2042981-001
2035570-001
2042214-001
32003587-002PCI Communications (DB-44)2.5 ft-
42003410-001BNC coax. Analog In (from Fluoro and so on)30 ft30V
52003410-001Analog Out (typically to Stimulator)30 ft30V
# Voltage rating of cables passing through conduits only
RF Ablation Device Interface.
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
Voltage
Rating
#
-
30V
300V
300V
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Page 87
TRAM/Amplifier Connections
Acquisition
System
3a
4
6
5
3b
2
1
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.
3a417335-xxxAdapter cable to TRAM. Part number varies by length ordered (-
3b *2016134-00115-pin to 9-pin adapter cable1 ft-
* These cables are contained in TRAMNet Cabling Kit (PN 2018683-001)
# Voltage rating of cables passing through conduits only
001 to -007)
4417335-002TRAM-RAC to Analog Output Box cable51 ft300V
417335-003TRAM-RAC to Analog Output Box cable70 ft300V
52007579-001IEB to Analog Output Box cable15 ft30V
62003434-001Amplifier to Acquisition system fiber optic cable75 ftN/A
Var iesVar ies
Rating
#
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Page 88
Equipment Overview
Acquisition
System
2
5
4
3
3b
1
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.
ItemPart NumberDescriptionLength
1418335-008Ethernet cable from PDM Base Station to Acquisition System100 ft400V
22062755-001CABLE, PDM TO ANOUT BOX15 ft-
32007579-001IEB to Analog Output Box cable15 ft-
42003434-001Amplifier to Acquisition system fiber optic cable75 ftN/A
52017098-001ePort PDM to Host5 ft-
# Voltage rating of cables passing through conduits only
2062755-002CABLE, PDM TO ANOUT BOX50 ft-
2062755-003CABLE, PDM TO ANOUT BOX75 ft-
2062755-004CABLE, PDM TO ANOUT BOX100 ft-
2017098-003ePort PDM to Host15 ft-
2017098-009ePort PDM to Host12.5 in-
2017098-005ePort PDM to Host25 ft-
2017098-007ePort PDM to Host45 ft-
2-54Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2097992-010D EN
Voltage
Rating
#
Page 89
PDM Base Station Plus/CO2 Connections
1
2
Typical Setup (with Capnostat 5 Mainstream CO2 Sensor)
Equipment Overview
Voltage
ItemPart NumberDescriptionLength
12077867-001PDM BASE STATION PLUSN/AN/A
22092608-001CAPNOSTAT 5 MAINSTREAM CO2 SENSOR10 ft-
Rating
#
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Page 90
Equipment Overview
1
3
2
Typical Setup (with LoFlo Sidestream CO2 Module)
ItemPart NumberDescriptionLength
12077867-001PDM BASE STATION PLUSN/A
22089969-001CABLE CO2 EXTENDER 4FT (OPTIONAL)4 ft
32092609-001C5 LOFLO SIDESTREAM CO2 MODULE2 ft
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Page 91
Amplifier/Stimulator Connections
IEB
Acquisition
MicroPace
Stimulator
MicroPace
CPU
Amplifier
RF
Generator
1
9
6
2
4
5
Catheter
Connection
Box
External
ECG
Auxiliary
Reference
3
7
8
Catheter
Input
Module
Personality
Module
Typical Setup (with MicroPace)
Equipment Overview
ItemPart NumberDescriptionLength
12003411-002BNC Cable. Connects back of MicroPace (ECG 1 Input) to back
50 ft300V
of IEB (Analog Out 1).
2N/ALarge Cable with D-Connectors. Connects back of MicroPace
N/AN/A
(Auxiliary Port) to side of Catheter Connection Box.
3N/ASmall Cable. Connects front of MicroPace (Green Connection
N/AN/A
Port or in emergencies Red Connection Port) to side of Catheter
Connection Box.
4301-00204-03
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
52003434-001Fiber Optic Cable75 ftN/A
62003587-002DB44 Connect Cable2.5 ft-
72003408-002Serial Cable50 ft30V
8301-00202-08Catheter Input Module8 ft-
# Voltage rating of cables passing through conduits only
Voltage
Rating
#
-
-
-
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Page 92
Equipment Overview
Typical Setup (with Bloom)
Personality
Module
RF
Generator
7
Acquisition
6
IEB
1
5
Bloom
Catheter
Input
Module
Catheter
8
4
Connection
Box
3
Amplifier
External
ECG
Auxiliary
Reference
ItemPart NumberDescriptionLength
12003410-001BNC Cable. Connects Bloom to back of IEB30 ft30V
2N/ALarge Cable with Square Connectors. Connects back of Bloom
to back of Patient Isolation Box.
3N/ASmall Cable. Connects front of Patient Isolation Box to side of
Catheter Connection Box.
4301-00204-03
301-00204-15
Red or Black leads connect to front of Catheter Connection Box
to Amplifier Stimulator Input.
301-00204-30
52003434-001Fiber Optic Cable75 ftN/A
62003587-002DB44 Connect Cable2.5 ft-
72003408-002Serial Cable50 ft30V
8301-00202-08Catheter Input Module8 ft-
# Voltage rating of cables passing through conduits only
Battery Battery
Patient
Isolation
Box
2
N/AN/A
N/AN/A
3 ft
15 ft
30 ft
Voltage
Rating
#
-
-
-
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Page 93
Equipment Setup
ItemPart NumberDescription
C and
C1
DN/APatient Isolation Box. Rear connection to Bloom (C1) via large cable with square
EN/ACatheter Connection Box. Side connection to the Patient Isolation Box (D) front
F2088700-002
Equipment Overview
N/ABloom (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
or
2088700-004
G301-00202-08Catheter Input Module. Catheter leads (not shown) plug into the block end. Connector on
1N/ABloom connection to IEB (BNC cable not shown).
2N/ABloom connection to Patient Isolation Box.
3N/APatient Isolation Box to Catheter Input Module Cable.
4301-00204-03Catheter Connection Box to Amplifier Cable.
52003425-001External ECG Connections. Colored leads connect to patient. Connector on other end
6301-00205-08Auxiliary Reference Cable. Plugs into the Amplifier (4) Auxiliary Input.
72003420-001ECG 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 94
Equipment Overview
Bloom (Connection Detail)
ItemDescription
1External Input: BNC connection to the IEB (cable not shown).
2J20: Connection to Patient Isolation Box (large square connector).
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Page 95
Audio
3
2
6
5
Local
Left
Speaker
Local
Right
Speaker
Remote
Left
Speaker
Remote
Right
Speaker
IEB
4
4
to 60601-1
Certified
Power
Supply
5
z440
1
Equipment Overview
ItemPart NumberDescription
12018218-001Y-connector (Connects to green jack on HP. One side to local speakers, the other to remote speakers.)
22018219-001Audio Isolator
32078970-001Speaker Set
42078970-001Speaker Power Supply (included with speakers)
52003927-001
62011108-002Speaker 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.
2097992-010D EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2-61
Page 96
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.
2097992-010D EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2-63
Page 98
Equipment Overview
Acquisition
System
1
CARTO System
Computer
ItemManufacturerPart NumberDescription
1GE2018217-001CAT5 Crossover Cable (25 ft).300V
Voltage
Rating
#
2-64Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2097992-010D EN
Page 99
Vivid Connections - CardioLab
WARNING: SHOCK HAZARD
Do not connect analog input or analog output cables to patient-isolated
equipment interfaces. This could compromise patient safety.
IEB
Vivid Remote
Trackball
Equipment Overview
HPz440
Computer
3b
3a
2a
2b
2c
ItemPart NumberDescriptionLength
1aN/ADVI to VGA Adapter
NOTE:This adapter must be used for proper image display
1b2032340-002Video Cable (The video cable from the Vivid should be
connected to DVI connector #4 on the Matrox KX-20 quad video
cable adapter using a regular DVI-to-VGA adapter - included
with the image capture board).
1c2047596-001VGA Video Connection ExtenderN/AN/A
2a2031919-001ECG Analog Output Cable100 ft *30V
2b2032673-001Vivid to Mac-Lab/CardioLab ECG Cable600 mm300V
2c2049942-001Ferrite Filter (locate 50 mm from Vivid side of ECG cable)N/AN/A
3a2031218-001USB to RS485 ConverterN/AN/A
3b2031215-001Remote Trackball Cable100 ft *300V
4N/AEthernet Cable (Can be connected to hospital network in the
procedure room or run through conduit to the control room.)
5N/AMatrox KX-20 Quad Video Adapter Cable (Included with the
image capture board)
* Run through conduit.
# Voltage rating of cables passing through conduits only
with the Vivid.
Vivid
1c
4
1b
1a
5
Voltage
N/AN/A
100 ft *30V
N/AN/A
N/AN/A
Rating
#
2097992-010D EN Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2-65
Page 100
Equipment Overview
Vivid Connections - Mac-Lab with TRAM
WARNING: SHOCK HAZARD
Do not connect analog input or analog output cables to patient-isolated
equipment interfaces. This could compromise patient safety.
Acquisition
System
Analog Output Box
5
TRAM-RAC
Vivid Remote
IEB
Trackball
6a
3b
2a
2b
1a
7
Vivid
2c
1b
1c
3a
IC
4
6b
Voltage
ItemPart NumberDescriptionLength
1aN/ADVI to VGA Adapter
N/AN/A
Rating
NOTE:This adapter must be used for proper image display
with the Vivid.
1b2032340-002Video Cable (The video cable from the Vivid should be
100 ft *30V
connected to DVI connector #4 on the Matrox KX-20 quad video
cable adapter using a regular DVI-to-VGA adapter - included
with the image capture board).
1c2047596-001VGA Video Connection ExtenderN/AN/A
2a2031919-001ECG Analog Output Cable100 ft *30V
2b2032673-001Vivid to Mac-Lab/CardioLab ECG Cable600 mmN/A
2c2049942-001Ferrite Filter (locate 50 mm from Vivid side of ECG cable)N/AN/A
3a2031218-001USB to RS485 ConverterN/AN/A
3b2031215-001Remote Trackball Cable100 ft *300V
4N/AEthernet Cable (Can be connected to hospital network in the
N/AN/A
procedure room or run through conduit to the control room.)
5417335-002TRAM-RAC to Analog Output Box Cable51 ft300V
417335-003TRAM-RAC to Analog Output Box Cable70 ft300V
#
6a2016134-00115-pin to 9-pin adapter cable1 ft-
6b417335-xxxAdapter cable to TRAM. Part number varies by length ordered (-
Var iesVar ies
001 to -007)
2-66Mac-Lab/CardioLab/Centricity Cardiology INW Service Manual2097992-010D EN
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