GE S5 Service Manual

							Table of figures
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List of tables
Table 1 Transference of parameters, Datex-Ohmeda monitors ............................................................ 32
Table 2 Transference of parameters, external monitors ....................................................................... 32
Table 3 DIS modules and interfaced devices ......................................................................................34
Table 4 Parameters transferred from S/5 Compact Anesthesia Monitor to S/5 Anesthesia 
Delivery Unit ......................................................................................................................... 39
Table 5 Events transferred from S/5 Anesthesia Delivery Unit to the S/5 Compact Anesthesia Monitor 40
Table 6 Parameters transferred from Dräger Cicero monitor to S/5 Compact Anesthesia Monitor or 
S/5 Compact Critical Care Monitor ........................................................................................ 41
Table 7 Parameters transferred from Dräger Cato, Julian and Narkomed 2C (NAD) monitor to the S/5 
Compact  Anesthesia Monitor or S/5 Compact Critical Care Monitor ....................................... 42
Table 8 Coding element connector, X4............................................................................................... 45
Table 9 Synchronization connector, X8 .............................................................................................. 45
Table 10 Signal output connector pin assignments .............................................................................. 46
Table 11 Patient simulators’ compatibility with each hemodynamic module.......................................... 49
Table 12 Adapter cables for hemodynamic patient simulators .............................................................. 50
Table 13 Guidance and manufacturer’s declaration – electromagnetic emissions ................................ B-1
Table 14 Guidance and manufacturer’s declaration – electromagnetic immunity ................................. B-2
Table 15 Guidance and manufacturer’s declaration – electromagnetic immunity ................................. B-3
Table 16 Recommended separation distances between portable and mobile RF communications 
equipment and the S/5™ CAM/ CCCM................................................................................. B-5 
						

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                                          Document no. M1031517-02
About this manual
Notes to the reader
This Technical Reference Manual is intended for service personnel and engineers who will install, 
service  and maintain  Datex-Ohmeda S/5 Compact Anesthesia Monitors running the software 
license L-CANE05 or L-CANE05A and S/5 Compact Critical Care Monitors running the software 
license L-CICU05 or L-CICU05A. 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 M1021567. 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,
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
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.  
						

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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 KeysNames of the hard keys on the Remote Controller, Command Board, side panel and modules are 
written in the following way: 
Others.
Menu ItemsSoftware terms that identify window par ts 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 iCentral Users Reference Manual: Alarms.
Hypertext linksHypertext links on PDF versions are written in blue color.
WARNING Warnings are written in the following way:
WARNINGThis 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 par ticular selection is not available in your system, the 
selection is shown grayed. 
Sign the check form after performing the procedure. 
						

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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: Inser t the WLAN PC 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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5
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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 transpor tation.
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 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.
PbNi-MH 
						

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1.1.3 Equipment safety symbols
- Attention, consult accompanying documents.
- When displayed next to the O2 value, indicates that the FiO2 low 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 par t 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.  
						

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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/NSerial 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 network (LAN). 
The monitor is connected to the wireless 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.
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 manufacture
Do not immerse the sensor in liquids.