Marquette UnityID Service manual

Unity Network

Interface Device (ID)

Service Manual

2009517-002 Revision A

127(Due to continuing product innovation, specifications in this manual are subject to change without notice.

Listed below are GE Medical Systems Information Technologies trademarks used in this document. All other trademarks contained herein are the property of their respective owners.

DASH and UNITY NETWORK are trademarks of GE Medical Systems Information Technologies registered in the United States Patent and Trademark Office.

Unity Network

Interface Device (ID) is a trademark of GE Medical Systems Information Technologies.

T-2 Unity Network ID Connectivity Revision A

2009517-002 20 November 2002

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

Manual Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Manual Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Naming Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3

Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4

Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5

Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5

Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-6

Equipment Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-6

Service Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7

Service Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

Equipment Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-7

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

System Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3

System Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3

Unity Network ID Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5

Interface Adapters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6

Supported Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

Anesthesia Machines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8

Continuous Cardiac Output Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9

Gas Analyzers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9

Infusion Pumps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-10

Patient Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-10

Pulse Oximeters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11

Transcutaneous Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12

Urometers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12

Ventilators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12

Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15

Performance Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-15

Environmental Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-15

Physical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-15

Certification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-16

Classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-16

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3 Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

Installation Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3

Special Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3

Communication Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3

Changing Internet Addresses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5

Connections for Stand-Alone Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . 3-9

Connections for Peripheral Mode of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

Monitor Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-10

Connection to Dash Pro 3000/4000 Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . .3-11

Connection to Solar 8000M/9500 Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-12

Peripheral Device Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14

Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-16

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

Maintenance Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3

Manufacturer Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3

Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3

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

Cleaning Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4

Exterior Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5

Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5

Power Outlet Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6

Ground (Earth) Integrity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6

Ground (Earth) Wire Leakage Current Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8

Enclosure Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9

Test Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-10

Checkout Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11

Test Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-11

Special Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-11

Peripheral Device Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-11

Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-12

Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-12

PM Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-13

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Repair Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14

5 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1

General Fault Isolation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Initial Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3

PC Communication Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3

Software Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3

Serviceability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3

Notification of Equipment Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4

Software Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-4

Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5

AC Line Voltage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6

120 VAC, 50/60 Hz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-6

240 VAC, 50/60 Hz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-6

Problems and Solutions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7

Status LED Displays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9

System Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-9

Peripheral Device Connection Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-10

6 Technical Replacement Units . . . . . . . . . . . . . . . . . . . . . 6-1

Ordering Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3

Technical Replacement Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3

Part Replacement Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4

Cover Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-4

PCB Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-6

Shipping Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9

7 Technical Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1

Theory of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3

Microprocessor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-4

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-5

Communication Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-6

Ethernet Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-7

Power Supply Conversion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8

ESD Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8

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Input and Output Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9

Ports 1 – 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-9

Ethernet Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-9

RS 232 Service Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-10

HyperTerminal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11

Special Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-11

Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-11

Using HyperTerminal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-12

Boot Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-13

Using the Boot Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-13

Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-15

Using the Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-15

Error and Event Log Menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-16

Exploded View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-18

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1 Introduction

Revision A Unity Network ID Connectivity Device 1-1

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For your notes

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Manual Informatio n

Revision History

Each page of this document has the document part number and revision letter at the bottom of the page. The revision letter changes whenever the document is updated.

Manual Purpose

This manual supplies technical information for service representatives and technical personnel so they can maintain the equipment to the assembly level. Use it as a guide for maintenance and electrical repairs considered technician repairable. Whe re necess ary the manua l identifie s additional sources of relevant information and technical assistance.

Introduction: Manual Information

Revision Date Comment

A 20 November 2002 Initial release.

Intended Audience

Naming Conventions

See the operator’s manual for the instructions necessary to operate the equipment safely in accordance with its function and intended use.

This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment.

In this manual, the Unity Network Interface Device (ID) is referred to as the Unity Network ID connectivity device.

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Definitions

Introduction: Manual Information

Black text Indicates keys on the keyboard, text to be entered, or h ardware items

such as buttons or switches on the equipment.

Italicized text Indicates software terms that identify menu items, buttons, or options

in various windows.

Ctrl+Esc Indicates a keyboard operation. A (+) sign between the names of two

keys indicates that you must press and hold 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.

<Space> Indicates you must press the spacebar. When instructions are given

for typing a precise text string with one or more spaces, the point where the spacebar must be pressed is indicated as: <Space>. The purpose of the < > brackets is to ensure you press the spacebar when required.

Enter Indicates you must press the “Enter” or “Return” key on the

keyboard. Do not type “enter”.

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Introduction: Safety Information

Safety Information

Responsibility of the Manuf acturer

GE Medical Systems Information Technologies is responsible for the effects of safety, reliability, and performance only if:

assembly operations, extensions, readjustments, modifications, or repairs are carrie d out by persons aut horized b y GE Medica l Systems Information Technologies, Inc.;

the electrical installation of the relevant room complies with the requirements of the appropriate regulations; and

the device is used in accordance with the instructions for use.

General

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

This device is not intended for home use. Federal law restricts this device to be sold by or on the order of a

physician. Contact GE Medical Systems Information Technologies before connecting

any devices or versions of devices not recommended in this manual to the connectivity device.

Parts and accessories used must meet t he requireme nts of t he appli cable IEC 60601 series sa fety st andard s, and/ or t he sy stem co nfigura tion mus t meet the requirements of the IEC 60601-1-1 medical electrical systems standard.

Periodically, and whenever the integrity of the device is in doubt, test all functions.

The use of ACCESSORY equipment not complying with the equivalent safety requirements of this equipment may lead to a reduced level of safety of the resulting system. Consideration relating to the choice shall include:

use of the accessory in the PATIENT VICINITY; and

evidence that the safety certification of the ACCESSORY has been performed in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1 harmonized national standard.

If the installation of the equipment, in the USA, will use 240V rather than 120V, the source must be a center-tapped, 240V, single-phase circuit.

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Introduction: Safety Information

001

002

003

4P41

004

Warnings, Cautions, and Notes

The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level of seriousness. Familiarize yourself with their definitions and significance.

Hazard is defined as a source of potential injury to a person. DANGER indicates an imminent hazard which, if not avoided, will

result in death or serious injury. WARNING indicates a potential hazard or unsafe practice which, if not

avoided, could result in death or serious injury. CAUTION indicates a potential hazard or unsafe practice which, if not

avoided, could result in minor personal injury or product/property damage.

NOTE provides application tips or other useful information to assure that you get the most from your equipment.

Equipment Symbols

The following symbols appear on the equipment.

ATTENTION: Consult accompanying documents before using the equipment.

Equipotentiality

Power:

l = ON; O = OFF

Medical Equipment With respect to electric shock, fire and mechanical hazards only in accordance with UL 2601-1, and CAN/CSA C22.2 NO. 601.1.

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Service Information

Service Requirements

Introduction: Service Information

Refer equipment servicing to GE Medical Systems Information Technologies authorized service personnel only.

Any unauthorized attempt to repair equipment under warr anty voids that warranty.

It is the user’s responsibility to report the need for service to GE Medical Systems Information Technologies or to one of it s au thor ized agents.

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.

Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be functional when required.

Equipment Identification

Every GE Medical Systems Information Technologies device has a unique serial number for identification. The serial number appears on the product label of each unit.

D 0 XX 0005 G XX

Month Manufactured

A = January B = February C = March D = April E = May F = June G = July H = August J = September K = October L = November M = December

Year Manufactured

0 = 2000 1 = 2001 2 = 2002 (and so on)

Product Code

Two-character product descriptor

Product Sequence Number

Manufacturing number (of total units manufactured)

Division

F = Cardiology G = Monitoring N = Freiburg Hellige

Device Characteristics

One or 2 letters that further describe the unit, for example: P = prototype not conforming to marketing specification R = refurbished equipment S = special product documented under Specials part numbers U = upgraded unit

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For your notes

Introduction: Service Information

1-8 Unity Network ID Connectivity Device Revision A

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2 Equipment Overview

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For your notes

2-2 Unity Network ID Connectivity Device Revision A

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Equipment Overview: System Components

System Components

System Operation

The Unity Network ID connectivity device acquires digital data from up to eight peripheral devices, processes this data, and transmits the formatted data to the monitoring network. The data can then be displayed on a clinical information system, central station, and/or GE Medical Systems Information Technologies patient monit or.

127(

Contact your GE Medical Systems Information Technologies representative for information about the monitors and software versions that are capable of receiving and displaying information from a Unity Network ID connectivity device.

Peripheral devices include anesthesia machines, continuous cardiac output monitors, gas analyzers, IV pumps, patient monitors, pulse oximeters, transcutaneous monitors, urometers, and ventilators.

Stand-Alone Mode

The Unity Network ID connectivity device operates in either a standalone mode or a peripheral mode of operation.

In the stand-alone mode, the Unity Network ID connectivity device provides data via the Unity Net work to one or more Unity Network devices capable of viewing remote patient data.

Unity Network ID

Interface Device

Central Station

Unity Monitoring Network

Peripheral

Adapter

Bedside Devices

Patient

Monitor

Clinical

Information

System

To Other

Unity Network

Devices

Network Gateway

To Clinical

Information

System

Network

PATIENT’S ROOM

005

The diagram is an example of patient data flow from peripheral devices to a clinical information system:

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Peripheral Mode

Equipment Overview: System Components

Each peripheral device requires a unique interface adapter to obtain the patient data.

Each adapter is connected by cabling to one of the eight peripheral device connectors on the Unity Network ID connectivity device.

The monitoring network delivers the patient data to a network gateway that segregates the monitoring network from the clinical information system. The gateway separates the real-time network and the transaction-oriented network to assure reliable delivery of real-time data.

The gateway sends the patient data to a clinical information system or other parts of the hospital’s enterprise-wide network.

In the peripheral mode, the Unity Network ID connectivity device provides its collected data to only one Unity Network device, such as a GE patient monitor. While in this mode, other viewing devices on the Unity Network cannot view data collected by the Unity Network ID connectivity device. This mode of operation allows for data collected by non-GE Medical Systems Information Technologies equipment to be merged with data collected locally by a GE patient monitor.

Peripheral Mode Operation Using Dash Pro Patient Monitor

PATIENTíSROOM

DashPro

PatientMonitor

UnityNetworkID

InterfaceDevice

Adapter

UnityMonitoringNetwork

Peripheral

Adapter

Bedside Devices

UnityNetwork

ToOther

Devices

006

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Equipment Overview: System Components

Peripheral Mode Operation Using Solar 8000M/9500 Monitor

PATIENTíSROOM

Solar8000M/9500

Monitor

M-PortNetwork

Unity Network ID Components

UnityNetworkID

InterfaceDevice

UnityMonitoringNetwork

Peripheral

Adapter

Bedside Devices

ToOther

UnityNetwork

Devices

034

Status LEDs

RS 232 Service Connector

Power Switch

Power Connector

The Unity Network ID connectivity device components include:

Peripheral Device Connectors

Ethernet Connector

RS 232 Service Connector—A dedicated serial port to communicate with a personal computer or terminal for configuration and programming.

Status LEDs— Eight bi-color light-emitting-diodes that indicate proper system function, peripheral device compatibility problems, and communication errors or delays.

Peripheral Device Connectors—Communication ports for eight peripher al de v ic e s.

Ethernet Connector—A single communication port for the monitoring network.

Power Connector—A receptacle for the AC power cord.

Power Switch—Power on/off switch with indicator light.

007

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Interface Adapters

Equipment Overview: System Components

&$87,21

Use of the wrong interface a d apter may cause improper operation of the supported peripheral device. Verify that the interface adapter on th e peripheral device is the correct adapter and is operational before the device is used on a patient.

Interface Adapters

008

Peripheral devices not manufactured by GE Medical Systems Information Technologies require a special interface adapter for connection to the Unity Network ID connectivity device. Dash Pro 3000/ 4000 monitors require a special interconnect cable with integral interface adapter. Interface adapters are available with different connector pin configurations and are specifically programmed to allow communication between the specific peripheral device and the Unity Network ID connectivity device.

127(

Solar 8000M/9000 monitors do not require the use of interface adapters for connection to the Unity Network ID connectivity de vice. These monitors utilize a direct Ethernet connection. Refer to the Installation chapter of this manual for further information.

127(

If your peripheral device software is updated, please complete and fax the software upgrade notification page found in this manual.

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Supported Devices

This section provides the li st of supported peripheral devices compatible with the Unity Network ID connectivity device. The devi ces are organized by type, and part numbers for the corresponding interface adapter are provided.

127(

Equipment Overview: Supported Devices

Due to continuous product innovation, this list may no longer be comprehensive. If necessary, call your sales representative for a current list of supported peripheral devices.

Refer to the host monitor operator documentation for further information about supported devices and monitored parameters.

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Anesthesia Machines

Equipment Overview: Supported Devices

Supported Anesthesia Machines

Supported Device

North American Dräger Medical Narkomed 2B Anesthesia Workstation

North American Dräger Medical Narkomed 2C Anesthesia Workstation

North American Dräger Medical Narkomed 2C (with CO2+Gas) Anesthesia Workstation

North American Dräger Medical Narkomed 3 Anesthesia Workstation

North American Dräger Medical Narkomed 4 Anesthesia Workstation

Supported Device

Software Version(s)

Narkomed 2B: 2.06 Narkomed 2C: 1.11E Narkomed 3: CO2/Agt: 1.02, O2 Med: 1.04, Oximeter: 1.07, Spiromed: 1.04, Sphymomed: 2.05, Baromed: 1.06, CCC: 1.01, ECC: 1.04, Alarms CRT: 2.02 Narkomed 4: 1.25 Comm hub: 2.01 Vitalert 2000: 2.05 Vitalert 3200: 1.08

Minimum

Unity Network

Waveform Parameter

— VNT V1A 420915-016

VNT Flow, VNT Pres

VNT Flow, VNT Pres, CO2 Exp

CO2 Exp VNT, Gas, CO2 V1A

VNT Flow, VNT Pres, CO2 Exp

VNT V1A

VNT, Gas, CO2 V1A

ID Software

For This

Interface

Part Number

For

Interface

Adapter

Dräger Medical Cato Anesthesia Machine

Dräger Medical PM8050 Anesthesia Machine

Dräger Medical Cicero PM8060 Anesthesia Machine (25 Pin)

Dräger Medical Cicero PM8060 Anesthesia Machine (9 Pin)

Dräger Medical Julian Anesthesia Machine

Dräger Medical Cicero EM Anesthesia Machine (25 Pin)

Dräger Medical Cicero EM Anesthesia Machine (9 Pin)

Dräger Medibus Version

3.00 and Device Version

2.02

Dräger Medibus Version

3.00 and Device Version

2.00

Dräger Medibus Version

3.00 and Device Version

2.00 Dräger Medibus Version

3.00 and Device Version

1.00 Dräger Medibus Version

3.00 and Device Version

2.00 Dräger Medibus Version

3.00 and Device Version

2.00

VNT Pres, CO2 Exp

VNT, Gas, CO2 V1A 420915-021

VNT, Gas, CO2 V1A 420915-036

VNT, Gas, CO2 V1A 420915-051

VNT, Gas, CO2 V1A 420915-038

VNT, Gas, CO2 V1A 420915-039

VNT, Gas, CO2 V1A 420915-044

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Equipment Overview: Supported Devices

Continuous Cardiac Output Monitors

Supported Continuous Cardiac Output Monitors

Supported Device

Baxter Edwards Vigilance CCO Monitor

Baxter Edwards Vigilance CCO Monitor (European)

Abbott Laboratories Q-Vue Monitor

Abbott Laboratories Q2 Monitor

Gas Analyzers

Minimum

Supported Device

Software Version(s)

Device v4.42, v5.02, v5.3 — CCO, SVO2 V1A 420915- 024

Device v4.42, v5.02, v5.3 — CCO, SVO2 V1A 420915-052

Q-Vue CCO Computer: Version 1.08, Application Version 1.08, and BIOS Version 1.03

Q2 Computer: Version 3.00, Application Version 3.00, and BIOS Version 1.07

Waveform Parameter

— CCO V1A 420915-025

— CCO, SVO2 V1A

Unity Network

ID Software

For This

Interface

Part Number

For

Interface

Adapter

Supported Device

Datex Capnomac Ultima Gas Analyzer

Datex Ohmeda Rascal II Anesthetic Gas Analyzer

Datex Ohmeda 5250 RGM (Respiratory Gas Monitor)

Nellcor Puritan Bennett N-1000 Pulse Oximeter

Nellcor Puritan Bennett N-2500 Pulse Oximeter (N-1000 and N-1500 combined)

Supported Gas Analyzers

Minimum

Supported Device

Software Version(s)

882916-2.0 882916-3.1

1.11 & 1.23 — Gas, CO2 V1A 420915-014

Display: 5.1 & 6.0 Signal: 5.007 & 6.007 ACX: 1.2

Display 2.03.03 (or 2.3) — Gas, CO2,

N-1000 Display: 2.03.03 (or 2.3) N-1500: 1.02.03 (or 1.2)

Waveform Parameter

— Gas, CO2 V1A 420915- 004

— Gas, CO2 V1A 420915-015

SPO2x

— Gas, CO2,

SPO2x

Unity Network

ID Software

For This

Interface

V1A 420915-034

V1A

Part Number

For

Interface

Adapter

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Infusion Pumps

Equipment Overview: Supported Devices

Supported Infusion Pumps

Minimum

Supported Device

Abbott Laboratories LifeCare 5000 Concurrent Flow Infusion System

Baxter Flo-Gard 6201 IV Pump

Baxter Flo-Gard 6301 IV Pump

Alaris Medical IVAC 560 0.21 — IV V1A 418265-028 Alaris Medical IVAC 570 0.09 IV V1A Alaris Medical IMED

Gemini PC-1 IV Pump Alaris Medical IMED

Gemini PC-2 IV Pump Alaris Medical IMED

Gemini PC-2TX IV Pump

Supported Device

Software Version(s)

1.6 — IV V1A 418265-026

1.04–1.13 — IV V1A 418265-027

1.08–1.11 — IV V1A

7.11 — IV V1A 418265-029

2.49a — IV V1A

2.31 — IV V1A

Waveform Parameter

Unity Network

ID Software

For This

Interface

Part Number

For

Interface

Adapter

Alaris Medical IMED Gemini PC-4 IV Pump

Patient Monitors

Supported Device

Hellige SMU EVO Patient Monitor

Siemens SC9000 Patient Monitor

1.31 — IV V1A

Supported Patient Monitors

Minimum

Supported Device

Software Version(s)

8.0E — Gas, CO2,

None Specified — CO2, SPO2x,

Waveform Parameter

SpO2x, TCO2, TCx, ECGx, RRx, NBPx, BPx, TMPx, BTCOx

ECGx, RRx, NBPx, BPx, TMPx, BTCOx

Unity Network

ID Software

For This

Interface

V1A 420915- 032

V1A 420915-035

Part Number

For

Interface

Adapter

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Pulse Oximeters

Equipment Overview: Supported Devices

Supported Pulse Oximeters

Supported Device

Nellcor Puritan Bennett N-200 Pulse Oximeter

Nellcor Puritan Bennett N-395 Pulse Oximeter

Nellcor Puritan Bennett N-1000 Pulse Oximeter

Nellcor Puritan Bennett N-2500 Pulse Oximeter (N-1000 and N-1500 combined)

Supported Device

Software Version(s)

Monitor Version 2.9 Powerbase Version 2.73

1.7.0.0, 1.8.0.0, 1.9.0.2,

1.9.3.0 Display 2.03.03 (or 2.3) — Gas, CO2,

N-1000 Display: 2.03.03 (or 2.3) N-1500: 1.02.03 (or 1.2)

Waveform Parameter

— SPO2x V1A 420915- 033

— SPO2x V1A 420915-069

SPO2x

— Gas, CO2,

SPO2x

Minimum

Unity Network

ID Software

For This

Interface

V1A 420915-034

V1A

Part Number

For

Interface

Adapter

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Equipment Overview: Supported Devices

Transcutaneous Monitors

Supported Transcutaneous Monitors

Supported Device

Novametrix Medical 840/860 TCO2M Monitors

Radiometer Medical TINA (TCM3) TCO2 Monitor

Urometers

Supported Device

Bard CritiCore 210/220 Urimeters

Minimum

Supported Device

Software Version(s)

3.3 TCO2M: eng-860-14

22 — TCO2 V1A 420915-023

Supported Urometers

Supported Device

Software Version(s)

Any — UO V1A 420915- 030

Waveform Parameter

— TCO2 V1A 420915- 022

Waveform Parameter

Unity Network

ID Software

For This

Interface

Minimum

Unity Network

ID Software

For This

Interface

Part Number

For

Interface

Adapter

Part Number

For

Interface

Adapter

Ventilators

Supported Device

Nellcor Puritan Bennett PB 840 Ventilator

Nellcor Puritan Bennett 7200 A/E/AE/SPE Adult Ventilators

Supported Ventilators

Minimum

Supported Device

Software Version(s)

4-070212-85-F (English) — VNT V1A 420915-063

26300-85-J (English) 24300-85-F (English) 26300-85-N (English) 26321-85-J (Spanish) 26322-85-E (French) 26323-85-G (German) 26324-85-K (Italian)

Waveform Parameter

— VNT V1A 420915- 001

Unity Network

ID Software

For This

Interface

Part Number

For

Interface

Adapter

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Equipment Overview: Supported Devices

Supported Ventilators

Nellcor Puritan Bennett Infant Star Neonatal Ventilator

Nellcor Puritan Bennett Infant Star 500 Neonatal Ventilator

Nellcor Puritan Bennett Infant Star 950 Neonatal Ventilator

Nellcor Puritan Bennett Adult Star, Adult Star 1500, and Adult Star 2000 Ventilators

Siemens Medical Servo Ventilator (SV) 300

Siemens Medical Servo Ventilator (SV) 900 C/D/E

Bear Medical Bear 1000 Ventilator

Hamilton Medical Veolar Ventilator

46 — VNT V1A 420915-008

49 and 107 — VNT V1A

107 — VNT V1A

216 and 218 — VNT V1A 420915-009

COM-PROM V2.0 COM-PROM V2.01

1.0 and 2.0 of Servo

VNT Flow,

VNT V1A 420915-011

VNT Pres

— VNT V1A 420915-002

Computer Module 990

9.7 and A3.3 VNT Flow,

VNT V1A 420915-005

VNT Pres

E V31E.4 N31D.2 R030.0 VNT Flow,

VNT V1A 420915-007

VNT Pres

Hamilton Medical Amadeus Ventilator

Hamilton Medical Galileo Ventilator

Drager Medical Babylog 8000/8000SC Infant Care Ventilator

Dräger Medical Evita Intensive Care Ventilator

Dräger Medical Evita 2 Intensive Care Ventilator

Dräger Medical Evita 2 Dura Intensive Care Ventilator

Dräger Medical Evita 4 Intensive Care Ventilator

Datex-Ohmeda Aestiva 3000 Anethesia Ventilator

Datex-Ohmeda 7800/7810 Anethesia Ventilators

A33X.0 N33A.6 R33A.0/ A33X.0 N33A.6 N01S.1

GMP01.21b GCP01.202 GPT01.00

Device v3.02, v4.02, v4.03, v4.04, and v5.00

VNT Flow, VNT Pres

VNT V1A

VNT V1A 420915-060

VNT V1A 420915-017

All with Medibus v3.00 Dräger Medibus Version

VNT Pres VNT V1A 420915-040

3.0 and Device Version 1.0 Dräger Medibus Version

4.0 and Device Version 1.0

Dräger Medibus Version

4.0 and Device Version 1.0

VNT Pres, CO2 Exp

VNT, CO2 V1A 420915-041

VNT, CO2 V1A 420915-042

VNT, CO2 V1A 420915-043

1.0 — VNT V1A 420915-050

1500-9001-000

— VNT V1A 420915-019

CATV00557

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Equipment Overview: Supported Devices

Supported Ventilators

Datex-Ohmeda 7900 Anethesia Ventilator

Bird VIP Infant-Pediatric, 6400ST, and 8400ST Ventilators

2.8 — VNT V1A 420915-049

Any V1A 420915-020

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Equipment Overview: Technical Specifications

Technical Specifications

Due to continuous product innovation, specifications for the Unity Network ID connectivity device are subject to change without notice. The following specifications are accurate as of the date of this publication.

Performance Specifications

Main Processor Motorola MC68EN360 25 MHz Network Type: Ethernet 10 BaseT Indicators Power: Green LED on AC switch

Status LEDs: Eight bicolor LEDs

Solid green indicates OK

Any other condition (color or state) indicates caution

Device Inputs Number: Eight devices

EIA Standard: RS-232 Baud Rates: 22 standard baud rates 50-115.2k

50, 75, 150, 200, 300, 450, 600, 900, 1200, 1800, 2400, 3600, 4800, 7200, 9600, 14.4k, 19.2k,

28.8, 38.4k, 57.6k, 115.2k Data Bits: 5 to 8 Stop Bits: 1 or 2 Parity: None, odd or even Connector: RJ-45 Device ID Facility: Interface adapter provides identification and connector adaptation for “plug and play”

Environmental Specifications

Power Requirements Input voltage: 90 -264 V ac; 50/60 Hz; Single Phase

Consumption: 7W Cooling: Natural Convention Heat Dissipation: 23.8 Btu/hr (7W)

Operating Conditions Temperature: 10°C to 40°C (50°F to 104 °F)

Humidity: 15% to 95% (noncondensing)

Storage Conditions Temperature: –40°C to 70°C (40°F to 158 °F)

Humidity: 15% to 95% (noncondensing)

Physical Specifications

Height 211 mm (8.3 in) Width 213 mm (8.4 in) Depth 66 mm (2.6 in) Weight 1.1 kg (2.4 lbs)

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Equipment Overview: Technical Specifications

4P41

004

Certification

Safety Standards Medical Equipment

With respect to electric shock, fire and mechanical hazards only in accordance with UL 2601-1, and CAN/CSA C22.2 NO. 601.1. EC 60601-1 certified. CE marking for the 93/42 EEC Medical Device Directive.

Separation Device The Unity Network ID connectivity device qualifies as a “Separation Device” as defined by the IEC

60601-1-1 Medical Electrical System Standard.

Classification

Type of protection against electrical shock

Degree of protection against electrical shock

Degree of protection against harmful ingress of water

Degree of safety of application in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide

Method(s) of sterilization or disinfection recommended by the manufacturer

Mode of operation Continuous operation

Class I

Not Applicable

Ordinary Equipment (enclosed equipment without protection against ingress of water)

Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.

Not Applicable

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+ 70 hidden pages

Marquette UnityID Service manual

Specifications and Main Features

Frequently Asked Questions

User Manual

Contents

1 Introduction

Manual Informatio n

Revision History

Manual Purpose

Intended Audience

Naming Conventions

Definitions

Safety Information

Responsibility of the Manuf acturer

General

Warnings, Cautions, and Notes

Equipment Symbols

Service Information

Service Requirements

Equipment Identification

2 Equipment Overview

System Components

System Operation

Unity Network ID Components

Interface Adapters

Supported Devices

Anesthesia Machines

Continuous Cardiac Output Monitors

Gas Analyzers

Infusion Pumps

Patient Monitors

Pulse Oximeters

Transcutaneous Monitors

Urometers

Ventilators

Technical Specifications

Performance Specifications

Environmental Specifications

Physical Specifications

Certification

Classification