GE Datex-Ohmeda S/5 Series Product manual

GE Healthcare
Datex-Ohmeda S/5TM Compact Anesthesia Monitor
Datex-Ohmeda S/5TM Compact Critical Care Monitor
Technical Reference Manual
Conformity according to the Council Directive 93/42/EEC concerning Medical Devices
CAUTION: U.S. Federal law restricts this device to sale by or on the order of a licensed medical practitioner.
Outside the USA, check local laws for any restriction that may apply.
All specifications subject to change without notice.
Order code M1065281
1st edition
June 2, 2008
GE Healthcare Finland Oy
Helsinki, Finland
P.O. Box 900
FI-00031 GE, FINLAND
Tel: [phone]
Fax: [phone]
www.gehealthcare.com
Copyright © 2008 General Electric Company. All rights reserved.
Datex-Ohmeda Inc.
P.O. Box 7550
Madison, WI 53707-7550, USA
Tel: [phone]
Fax: [phone]

Intended purpose (Indications for use)
The Datex-Ohmeda S/5 Compact Anesthesia Monitor with L-CANE06 or L-CANE06A software is intended
for multiparameter patient monitoring with optional patient care documentation.
The S/5 Compact Anesthesia Monitor with L-CANE06 or L-CANE06A software is indicated for monitoring of
hemodynamic (including arrhythmia and ST-segment analysis), respiratory, ventilatory,
gastrointestinal/regional perfusion, Bispectral index (BIS), Entropy (State Entropy and Response Entropy)
and neurophysiological status of all hospital patients.
The S/5 Compact Anesthesia Monitor with L-CANE06 and L-CANE06A software when using BIS is for
monitoring the state of the brain by data acquisition and processing of electroencephalograph signals
and may be used as an aid in monitoring the effects of certain anesthetic agents.
The S/5 Compact Anesthesia Monitor with L-CANE06 or L-CANE06A software is also indicated for
documenting patient care related information.
The S/5 Compact Anesthesia Monitor with L-CANE06 or L-CANE06A software is indicated for use by
qualified medical personnel only.
The Datex-Ohmeda S/5 Compact Critical Care Monitor with L-CICU06 or L-CICU06A software is intended
for multiparameter patient monitoring.
The S/5 Compact Critical Care Monitor with L-CICU06 and L-CICU06A software is indicated for monitoring
of hemodynamic (including arrhythmia and ST-segment analysis), respiratory, ventilatory,
gastrointestinal/regional perfusion, Bispectral index (BIS) and neurophysiological status of all hospital
patients.
The S/5 Compact Critical Care Monitor with L-CICU06 and L-CICU06A software when using BIS is for
monitoring the state of the brain by data acquisition and processing of electroencephalograph signals
and may be used as an aid in monitoring the effects of certain anesthetic agents.
The S/5 Compact Critical Care Monitor with L-CICU06 and L-CICU06A software is indicated for use by
qualified medical personnel only.
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 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.
In accordance with IEC 60529
In accordance with EU Medical Device Directive
The Datex-Ohmeda S/5 Compact Anesthesia Monitor is classified as IIb.
The Datex-Ohmeda S/5 Compact Critical Care Monitor is classified as 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.
Responsibility of the manufacturer
GE Healthcare Finland Oy (GE) is responsible for the effects on safety, reliability and performance of the
equipment only if:
• assembly, extensions, readjustments, modifications, servicing and repairs are carried out by
personnel authorized by GE.
• the electrical installation of the monitor room complies with appropriate requirements.
• the equipment is used in accordance with the "User's Guide" and serviced and maintained in
accordance with the “Technical Reference Manual”.
Trademarks
Datex, Ohmeda, S/5, D-lite, D-lite+, Pedi-lite, Pedi-lite+, D-fend, D-fend+, Mini D-fend, OxyTip+, MemCard,
ComWheel, ComBar, EarSat, FingerSat, FlexSat, PatientO2, Patient Spirometry, Entropy and Tonometrics
are trademarks of GE Healthcare Finland Oy. All other product and company names are property of their
respective owners.
A portion of the Entropy software is derived from the RSA Data Security, Inc. MD5 Message-Digest
Algorithm.

Product availability
Some of the products mentioned in this manual may not be available in all countries.
Please, consult your local representative for the availability.

Master Table of Contents
1
Document no. M1144951-004
Datex-Ohmeda
S/5TM Compact Anesthesia Monitor
S/5TM Compact Critical Care Monitor
Technical Reference Manual, Order code: M1065281
1st edition
Part I, General Service Guide
Part II, Product Service Guide
Document No. Updated Description
M1144951 -004 Introduction, System description, Installation,
Interfacing, Functional check, General
troubleshooting
1
M1144953 -001 Planned Maintenance Instructions 2
Document No. Updated Description
M1144955 -001 CAM, CCCM Service Menu 1
M1144956 -003 Display Unit for F-CM1, F-CMC1 rev. 00...05
F-CMREC1, F-CMCREC1 rev .00...01
Software Licenses L-CANE06(A), L-CICU06(A)
2
M1144958 -001 Frame Unit for F-CM1, F-CMC1 rev. 00...05
F-CMREC1, F-CMCREC1 rev. 00...01
AC/DC Power Supply Unit
3
M1144959 -001 Spare parts 4

Datex-Ohmeda S/5 Compact Anesthesia and Compact Critical Care Monitors
2
Document no. M1144951-004
For your notes:

Table of contents
i
Document no. M1144951-004
Table of contents
Table of contents i
Table of figures iv
About this manual 1
1Introduction 3
1.1 Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.1.1 Symbols on transport packaging. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.1.2 Symbols on equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.1.3 Equipment safety symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.1.4 Other symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
1.2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
1.2.1 Safety precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
1.2.2 ESD precautionary procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
1.2.3 Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
2 System description 15
2.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
2.2 Bus structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
2.3 Distributed processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
2.4 Module communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
2.5 Software loading. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
2.6 Parameter modules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
3 System installation 19
3.1 Unpacking instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
3.2 Choosing location. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
3.3 S/5 Frame for Compact Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
3.3.1 Compact Monitor connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
3.3.2 Connecting to mains . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
3.3.3 Connecting to Network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
3.3.4 Connecting to Wireless Network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
3.3.5 Inserting the parameter modules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
3.3.6 E-PSM(P) Mounting Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
3.3.7 Downloading Monitor Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
3.3.8 Performing Factory Reset. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
3.3.9 Installing the Datex-Ohmeda Network and MemCard Upgrade, U-CMMEM . . . . . . . 26
3.3.10 Installing the Datex-Ohmeda Network Upgrade, U-CMNET . . . . . . . . . . . . . . . . . . . . . . 27
3.3.11 Installing the S/5 Wireless LAN Upgrade, U-CMW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
3.3.12 Installing the S/5 Recorder Upgrade, U-CMREC1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
3.4 S/5 Remote Controller, K-CREMCO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
3.5 Anesthesia Record Keeping Keyboard, K-ARKB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
3.6 ARK Barcode Reader, N-SCAN (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
3.6.1 Connection to Compact Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Datex-Ohmeda S/5 Compact Anesthesia and Compact Critical Care Monitors
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Document no. M1144951-004
3.7 S/5 Compact Airway Modules, E-xxxx / M-xxxxx . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
3.7.1 Sample gas exhaust . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
3.7.2 Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
4Interfacing 35
4.1 Interfacing external monitors via Interface Module, E-INT / M-INT . . . . . . . . . . . . . . . . . . . . . . 35
4.1.1 Connection to external Datex-Ohmeda monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
4.1.2 Connection to Critikon Dinamap 1846SX, Abbott Oximetrix 3 and Baxter Explorer 37
4.1.3 Connection to Baxter Vigilance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.1.4 Connection to Nellcor N-100 and N-1000. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.1.5 Connection to Nellcor N-200 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.2 Interfacing external bedside devices via Device Interfacing Solutions, N-DISxxx. . . . . . . . 38
4.2.1 Device Interfacing Solution components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
4.2.2 Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
4.2.3 Mounting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
4.2.4 Selecting the external device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
4.2.5 Functional check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
4.2.6 Selecting the parameter data source. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
4.3 Interfacing Datex-Ohmeda Anesthesia Delivery Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
4.3.1 Interconnection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
4.3.2 Setting interfacing parameters on the S/5 Anesthesia Delivery Unit. . . . . . . . . . . . . . 43
4.3.3 Setting interfacing parameters on the S/5 Compact Anesthesia Monitor . . . . . . . . . 43
4.4 Interfacing Dräger Cicero, Cato, Julian and Narkomed 2C (by NAD) . . . . . . . . . . . . . . . . . . . . 44
4.4.1 Interconnection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
4.4.2 Setting communication parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
4.4.3 Setting interfacing parameters on the S/5 Compact Anesthesia Monitor or
S/5 Compact Critical Care Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
4.5 Interfacing printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5.1 Setting S/5 Compact Monitor interface for printers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5.2 Connection to serial printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5.3 Connection to parallel printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5.4 Installing the Serial-to-Parallel Converter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5.5 Connection to printer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
4.6 Interfacing computer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
4.7 Output signals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
4.7.1 Digital outputs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
4.7.2 Analog outputs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
4.7.3 S/5 Pressure Temp Module, E-PT or M-PT, output signals . . . . . . . . . . . . . . . . . . . . . . . . 51
5 Functional check 53
5.1 Recommended tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
5.1.1 Hemodynamic patient simulators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
5.2 Visual inspection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
5.3 Functional inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
5.3.1 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
5.3.2 Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
5.3.3 Keyboard(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
5.3.4 Frame unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
5.3.5 Display unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

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Document no. M1144951-004
5.3.6 Compact Airway Module, E-CXXXXX/ M-CXXXXX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
5.3.7 Single width Airway Module, E-miniC/ M-miniC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
5.3.8 Tonometry Module, E-TONO/ M-TONO. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
5.3.9 Multiparameter Hemodynamic Modules. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
5.3.10 Pressure/Pressure Temp Modules, E-P, E-PT, M-P, M-PT . . . . . . . . . . . . . . . . . . . . . . . . . . 60
5.3.11 Dual pressure Module, E-PP/ M-PP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
5.3.12 Cardiac Output Modules, E-COP/ M-COP, E-COPSv/ M-COPSv . . . . . . . . . . . . . . . . . . . . 61
5.3.13 NIBP module, M-NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
5.3.14 Nellcor Compatible Saturation module, E-NSATX/ E-NSAT/ M-NSAT . . . . . . . . . . . . . . 61
5.3.15 Datex-Ohmeda Oxygen Saturation module, M-OSAT . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.3.16 BIS Module, E-BIS/ M-BIS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.3.17 Entropy Module, E-ENTROPY/ M-ENTROPY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.3.18 Data Card and Menu Card function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.3.19 Recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.3.20 Network connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3.21 Wireless Network Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3.22 Interface Module, E-INT/ M-INT. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3.23 Interface module for PSM, E-INTPSM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3.24 Device Interfacing Solution, N-DISxxx . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3.25 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
6 General troubleshooting 65
6.1 Software troubleshooting chart. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Appendix A: Functional check form, Datex-Ohmeda S/5 CAM, CCCM A-1
Appendix B: ElectroMagnetic Compatibility B-1
Appendix C: Channel Mask Selections C-1

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Table of figures
Figure 1 S/5 Compact Anesthesia Monitor system........................................................................................................................ 3
Figure 2 General bus structure of S/5 system................................................................................................................................15
Figure 3 Principle of UPI section operation ......................................................................................................................................16
Figure 4 General structure of parameter modules with patient isolation.........................................................................17
Figure 5 External connections of Compact Monitor frame F-CM(C)1 rev.05 ....................................................................20
Figure 6 External connections of Compact Monitor frame F-CM(C)1 rev.00...03............................................................21
Figure 7 E-PSM(P) mounting accessories ..........................................................................................................................................24
Figure 8 Installation of the U-CMREC1 ...............................................................................................................................................29
Figure 9 ARK Barcode Reader, N-SCAN connected to Compact Monitor ..........................................................................30
Figure 10 Compact Airway Module, E-XXXX.......................................................................................................................................30
Figure 11 Scavenging through ventilator reservoir ........................................................................................................................31
Figure 12 Connecting the gas module to the scavenging connector of S/5 Avance .....................................................32
Figure 13 Sample gas returned to patient circuit in ADU.............................................................................................................33
Figure 14 Connection cables and LED indicators ............................................................................................................................40
Figure 15 An example of interfacing external devices with Device Interfacing Solution..............................................41
Figure 16 Connecting S/5 Compact Monitor to printer, converter model PI130-R2 .......................................................48
Figure 17 Connecting S/5 Compact Monitor to printer, converter model PI 1115A........................................................49
Figure 18 S/5 Compact Monitor general troubleshooting flowchart......................................................................................65
Figure 19 Software troubleshooting ......................................................................................................................................................66

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Document no. M1144951-004
About this manual
Intended audience
This Technical reference manual is meant for service representatives and technical personnel
who install, configure, maintain, administer, troubleshoot or repair Datex-Ohmeda S/5 Compact
Anesthesia Monitors running the software license L-CANE06 or L-CANE06A and S/5 Compact
Critical Care Monitors running the software license L-CICU06 or L-CICU06A.
Notes to the reader
As the monitor setup may vary, some functions described may not be available in the monitor
you are using.
•The order code for the entire printed manual is M1065281. The manual includes
Technical Reference Manual Slots and every slot has an individual document number.
•Part I gives the reader an overview of the monitor. It contains the information needed to
install, interface and troubleshoot the monitors. Instructions for functional check and
planned maintenance are also included. Read the manual through and make sure that
you understand the procedures described before the installation of the monitor. To avoid
risks concerning safety or health, strictly observe the warning indications. If you need
any assistance concerning the installation, please do not hesitate to contact your
authorized distributor.
•Part II contains detailed descriptions of each component of the S/5 CAM, CCCM Monitor,
such as frame unit, parameter modules Remote Controller and Device Interfacing
Solution. Service check for each product, service menus and all the spare parts
information for the Monitor is included.
For information of parameter modules, Remote Controller and Device Interfacing Solution refer
to the “S/5 E-Modules, Technical Reference Manual”. Service check for each of these products
is included in these slots.
The manufacturer reserves the right to change product specifications without prior notice.
Although the information in this manual is believed to be accurate and reliable, the
manufacturer assumes no responsibility for its use.
Installation and service are allowed by authorized service personnel only.
GE Healthcare Finland Oy (GE) assumes no responsibility for the use or reliability of its software
in equipment that is not furnished by GE.
Related documentation
S/5 Modules
S/5 E-Modules, Technical Reference Manual
S/5 M-Modules, Technical Reference Manual
S/5 Compact Anesthesia Monitor
For instructions for daily use including cleaning and daily maintenance, clinical aspects and
basic methods of measurement see:
S/5 Compact Anesthesia Monitor, User’s Guide
S/5 Compact Anesthesia Monitor, User’s Reference Manual

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S/5 Compact Critical Care Monitor
For instructions for daily use including cleaning and daily maintenance, clinical aspects and
basic methods of measurement:
S/5 Compact Critical Care Monitors, User’s Guide
S/5 Compact Critical Care Monitors, User’s Reference Manual
For more information about the iCentral, S/5 Arrhythmia Workstation and anesthesia record
keeping solution, see the “Technical Reference Manuals” and “User’s Reference Manuals” for
these products.”
Software options and default settings are described in the “Default Configuration Worksheet”
delivered with each monitor.
Available accessories are described in the “Supplies and Accessories” catalog delivered with
each monitor.
Conventions used
To help you find and interpret information easily, the manual uses consistent text formats:
Hard Keys Names of the hard keys on the Remote Controller, Command Board, side panel and modules
are written in the following way: Others.
Menu Items Software terms that identify window parts or menu items are written in bold italic: ECG Setup.
Menu access is described from top to bottom. For example, the selection of the Monitor
Setup hard key, the Screen 1 Setup menu item and the Waveform Fields menu item would be
shown as Monitor Setup - Screen 1 Setup - Waveform Fields.
‘Messages’ Messages (alarm messages, informative messages) displayed on the screen are written inside
single quotes: ‘Please wait’.
“Sections” When referring to different sections in this manual or to other manuals, manual names and
section names are enclosed in double quotes:
See section "Cleaning and care."
Please refer to "User's Reference Manual: Alarms."
Hypertext links Hypertext links on PDF versions are written in blue color.
WARNING Warnings are written in the following way:
WARNING This is a WARNING.
CAUTION Cautions are written in the following way:
CAUTION This is a CAUTION.
NOTE Notes are written in the following way:
NOTE: This is a NOTE.
In this manual, the word “select” means choosing and confirming.
Illustrations and names
All illustrations in this manual are only examples, and may not necessarily reflect your system
settings or data displayed in your system. If a particular selection is not available in your
system, the selection is shown grayed.
"Sign the check form after performing the procedure.

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Document no. M1144951-004
1 Introduction
The modular design makes the system flexible and easy to upgrade. In addition to patient
parameter modularity and easy upgrades, the monitor can be upgraded to anesthesia record
keeping, wired and wireless networking and memory card operation. Additionally, external
devices can be interfaced to the monitor with interface modules.
NOTE: Your system may not include all these components. Consult your local representative
for the available components.
Figure 1 S/5 Compact Anesthesia Monitor system
(1) S/5 Compact Anesthesia Monitor with modules inside
(2) Remote Controller, K-CREMCO
(3) Printer
(4) Wireless Network (WLAN) Access Point, N-WAP
(5) Network (LAN)
Optional components
Optional components are:
•Built-in recorder, N-CMREC1
•Remote controller
•Keyboard for anesthesia record keeping solution, barcode reader
•Wireless network option, N-CMW
Possible software options are:
•MemCard option, N-CMMEM
NOTE: Insert the WLAN card in the first slot from the front.
NOTE: Memory Module, M-MEM/ E-MEM, is not compatible with the S/5 Compact Monitors.
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Communication between monitors
You can use the Compact Monitor as a stand-alone monitor or for:
−viewing and receiving data (alarms, vital signs) from other patient monitors
−gathering and storing data during transportation.
To view other patient monitors, the monitor needs to be connected to the network (LAN or
WLAN). To gather, store, and transfer data between different Datex-Ohmeda monitors, use
memory cards or connect the monitor to the network.
NOTE: With WLAN, use only Data Card.

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1.1 Symbols
1.1.1 Symbols on transport packaging
1.1.2 Symbols on equipment
The contents of the transport package are fragile and must be handled with
care.
Indicates the correct upright position of the transport package.
The transport package must be kept in a dry environment.
Indicates the temperature limitations within which the transport package
should be stored.
This package can be recycled.
This battery contains Ni-MH and can be recycled.
Dangerous voltage.
When using the ARK Barcode Reader, N-SCAN, do not stare into beam. The N-SCAN
Barcode Reader is a Class 2 laser product.
Pb
Ni-MH

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1.1.3 Equipment safety symbols
- Attention, consult accompanying documents.
- When displayed next to the O2value, indicates that the FiO2low alarm limit
is set below 21%.
- When displayed next to the HR value, indicates that the pacer is set on R.
- On the modules or frames indicates that modules with identical
measurements should not be used in the same monitor. If such modules
have been inserted, remove the module that has been most recently
connected. You can also remove both modules and re-connect the new
module after five seconds.
- On the Interface Module E-INT, M-INT, indicates that it is for connecting
external devices. Do not connect patient cables to the module.
- On the E-TONO, M-TONO module indicates that the module should only be
used with Tonometrics catheters.
- On the E-miniC module indicates that airway gases should be calibrated
every six months in normal use and every two months in continuous use.
- BIS: On the Aspect DSC indicates that the converter must not be opened for
any reason or autoclaved.
- On the E-PRESTN, E-PRETN, E-RESTN, E-PSM, E-PSMP, E-P, E-PP, E-PT, E-COP
and E-COPSv module indicates that protection against cardiac defibrillator
discharge is due in part to the accessories for pulse oximetry (SpO2),
temperature (T) and invasive pressure (P) measurement.
- On the E-NMT, M-NMT module indicates the following warnings:
- Do not place the NMT stimulating electrodes on the patient’s chest.
- Always stop the NMT measurement before handling the stimulating
electrodes.
- Never subject a patient with an implanted electronic device to electrical
stimulation without consulting a medical specialist first.
- On the rear or bottom panel this symbol indicates the following warnings
and cautions:
- Electric shock hazard. Do not open the cover or the back. Refer servicing
to qualified service personnel.
- For continued protection against fire hazard, replace the fuse only with
one of the same type and rating.
- Do not touch a battery-operated monitor during defibrillation procedure.
- Disconnect from the power supply before servicing.
- Do not use the monitor without manufacturer approved mounting
attached.
- Lithium battery on the CPU board: follow the regional regulations for
disposal.

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1.1.4 Other symbols
Type BF (IEC 60601-1) protection against electric shock.
Type BF (IEC 60601-1) defibrillator-proof protection against electric shock.
Type CF (IEC 60601-1) protection against electric shock.
Type CF (IEC 60601-1) defibrillator-proof protection against electric shock.
When displayed in the upper left corner of the screen, indicates that the alarms
are silenced. When displayed in the menu or digit fields, indicates that the alarm
source has been turned off or alarm does not meet the alarm-specific activation
criteria.
ESD warning symbol for electrostatic sensitive devices. Pins of connectors
identified with the ESD warning symbol should not be touched. Connections
should not be made to these connectors unless ESD precautionary procedures
are used. For details, see section “1.2.2. ESD precautionary procedures”.
Symbol for non-ionizing electromagnetic radiation. Interference may occur in
the vicinity of equipment marked with this symbol.
Equipotentiality. Monitor can be connected to potential equalization
conductor.
Alternating current
Fuse. Replace the fuse only with one of the same type and rating.
SN, S/N Serial Number
Battery operation and remaining capacity (green bar)
Battery charging (white bar)
Submenu. Selecting an alternative marked with this symbol in a menu opens a
new menu.

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The monitor is connected to the Datex-Ohmeda Network (LAN).
The monitor is connected to the Datex-Ohmeda Network (WLAN).
Data Card (green) and/or Menu Card (white) is inserted.
WLAN signal strength. The number of segments corresponds to the signal
strength: four segments indicate strong signal, one segment weak signal.
When connection to access point is being searched, the segments scroll from
zero to four and back.
Ethernet connector
A blinking heart next to the heart rate or pulse rate value indicates the beats
detected.
A lung next to the respiration rate value indicates that respiration rate is
calculated from the impedance respiration measurement.
Gas inlet
Gas outlet
Do not reuse.
Use by. Indicates the last use day.
Date of manufacturer
Does not contain Latex.
Do not immerse the sensor in liquids.

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IPX class:
IPX0
IPX1
IPX2
IPX3
IPX4
IPX7
IPX8
Degree of protection against harmful ingress of water as detailed in the
IEC 60529:
- Ordinary equipment
- Protection against vertically falling water drops.
- Protection against vertically falling water drops when enclosure tilted
up to 15 °.
- Protected against spraying water.
- Protected against splashing water.
- Protected against the effects of temporary immersion in water.
- Protected against the effects of continuous immersion in water.
This symbol 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.
This symbol indicates the product contains hazardous materials in excess of
the limits established by the Chinese standard SJ/T11364-2006 Requirements
for Concentration Limits for Certain Hazardous Substances in Electronic
Information Products. The number in the symbols is the Environment-friendly
Use Period (EFUP), which indicates the period during which the toxic or
hazardous substances or elements contained in electronic information
products will not leak or mutate under normal conditions so that the use of
such electronic information products will not result in any severe
environmental pollution, any bodily injury or damage to any assets. The unit of
the period is “Year”.
In order to maintain the declared EFUP, the product shall be operated normally
according to the instructions and environmental conditions as defined in the
product manual, and the periodic maintenance schedules specified in Product
Maintenance Procedures shall be followed strictly.
Consumables or certain parts may have their own label with an EFUP value
less than the product. Periodic replacement of those consumables or parts to
maintain the declared EFUP shall be done in accordance with the Product
Maintenance Procedures.
This product must not be disposed of as unsorted municipal waste, and must
be collected separately and handled properly after decommissioning.
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1.2 Safety
The following list contains general warnings and cautions you should know before installing,
maintaining or servicing the system. Warnings and cautions specific to the use of the system
can be found in the User’s Guide and User’s Reference Manual.
1.2.1 Safety precautions
Warnings
WARNING A WARNING indicates a situation in which the user or the patient may be in
danger of injury or death.
•The device is not able to withstand unpacked drops from a height of 1 m without
damaging the module latches. If the device is dropped, please service the device before
taking it back into use.
Power connection
•Always check that the power cord and plug are intact and undamaged.
•Use only hospital-grade grounded power outlets and power cord. Do not remove the
grounding pin from the power plug.
•Use only an intact power cord. Replace the power cord if it is cracked, frayed, broken or
otherwise damaged.
•Do not apply tension to the power cord otherwise the cord may get damaged.
•Do not use an additional multiple socket outlet, extension cord or adapters of any kind.
•Before starting to use the system, ensure that the whole combination complies with the
international standard IEC 60601-1-1 and with the requirements of the local authorities.
Do not connect any external devices to the system other than those specified.
•If the integrity of the external protective earth conductor arrangement is in doubt, use the
monitor with battery operation.
•To avoid the risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
Installation
•Keep the monitor horizontal when the Compact Airway Module is used. Tilting the monitor
may cause erroneous results in the Compact Airway Module’s readings and damage the
module.
•The monitor or its components should not be used adjacent to or stacked with other
equipment. If adjacent or stacked use is necessary, the monitor and its components
should be observed to verify normal operation in the configuration in which it will be
used.
•Pins of connectors identified with the ESD warning symbol should not be touched.
Connections should not be made to these connectors unless ESD precautionary
procedures are used. For details, see section “1.2.2. ESD precautionary procedures”
•After transferring or reinstalling the monitor, always check that it is properly connected
and all parts are securely attached. Pay special attention to this in case of stacked
mounting.
•Do not use the monitor in high electromagnetic fields (for example, during MRI.)
•Never install the monitor so that it is above the patient.