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GE Healthcare

Patient Monitor B40 Technical Reference Manual

GE Healthcare Patient Monitor B40 Technical Reference Manual Patient Monitor B40 English 2062472-001 H (Paper) ©
GE Healthcare Patient Monitor B40 Technical Reference Manual Patient Monitor B40 English 2062472-001 H (Paper) ©

Patient Monitor B40 English 2062472-001 H (Paper) © 2013 General Electric Company. All Rights Reserved.

Patient Monitor B40

Technical Reference Manual

Patient Monitor B40 Technical Reference Manual 0459 Conformity according to the Council Directive 93/42/EEC concerning

0459

Conformity according to the Council Directive 93/42/EEC concerning Medical Devices

All specifications subject to change without notice.

Order code 2062472-001

Revision H

4 March, 2013

GE Medical Systems Information Technologies, Inc. 8200 West Tower Avenue Milwaukee, WI USA Zip: 53223 Tel: 1 414 355 5000 (outside US) 800 558 5102 (US only) Fax: 1 414 355 3790 www.gehealthcare.com Copyright © 2013 General Electric Company. All rights reserved.

GE Healthcare

3F Building 1, GE Technology Park

1 Huatuo Road

Shanghai PRC 201203

Tel: +86 21 3877 7888 Fax: +86 21 3877 7451

Classifications

In accordance with IEC 60601-1

Class I and internally powered equipment - the type of protection against electric shock.

Type BF or CF equipment. The degree of protection against electric shock is indicated by a symbol on each parameter module.

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

Continuous operation according to the mode of operation.

Portable Monitor

In accordance with IEC 60529

IP21 - degree of protection against harmful ingress of water.

In accordance with EU Medical Device Directive

IIb.

In accordance with CISPR 11:

Group 1 Class A;

Group 1 contains all ISM (Industrial, scientific and medical) equipment in which there is intentionally generated and/or used conductively coupled radio-frequency energy which is necessary for the internal functioning of the equipment itself.

Class A equipment is equipment suitable for use in all establishments other than domestic and those directly connected to a low-voltage power supply network which supplies buildings used for domestic purposes.

Trademarks

Listed below are GE Medical Systems Information Technologies and GE Healthcare Finland Oy

trademarks used in this document. All other product and company names contained herein

are the property of their respective owners.

Datex, Ohmeda, DINAMAP, Trim Knob, Unity Network, CARESCAPE, EK-Pro, TruSignal, Entropy, GE Healthcare, GE Medical system, General Electric Company.

1

Introduction

About this manual

 

1

1 Overview

3

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4

1.2 Safety

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1.2.1

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8

1.2.2

Safety message signal words

 

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8

1.2.3

Safety precautions

 

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1.2.4

ESD precautionary

 

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1.2.5

Disposal

 

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10

1.3 Service information

 

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10

1.3.1 Service

 

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1.3.2 Equipment identification

 

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2 System description

 

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2.1 Introduction

 

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11

2.2 Bus structure

 

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11

2.3 Distributed processing

 

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12

2.4 Module

 

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2.4.1

Serial communication

 

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12

2.5 Parameter modules

 

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13

2.6 Software loading

 

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13

3 Frame functional description

 

14

3.1 Main components

 

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14

3.1.1

Keyboards

 

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14

3.1.2

Display

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14

3.1.3

CPU board

 

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16

3.1.4

Power board

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17

3.1.5

AC/DC unit

 

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19

3.1.6

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19

3.2 Interfacing computer

 

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19

3.3 Connectors and

signals

 

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20

3.3.1

External

 

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20

4 Hemo-dynamic module introduction

 

23

4.1 Monitor software compatibility

 

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23

4.2 Main components

 

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23

4.2.1 Hemo-dynamic module

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23

4.2.2 Signals and isolation barrier

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24

4.2.3 Power supply

 

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24

4.2.4 NIBP board

 

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25

4.2.5 ECG board in 5-lead

 

27

4.2.6 STP board

 

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