S5 FM Technical Reference Manual 3rd edition February 2012

Indications for use The S/5 FM with L-FICU06 and L-FICU06A and N-FCREC Module are intended for multiparameter patient monitoring. The S/5 FM with L-FICU06 or L-FICU06A software is indicated for monitoring of hemodynamics (including arrhythmia and ST-segment analysis) and respiratory status of all hospital patients. Extension module N-FCREC (option N-FCREC or N-FC) is indicated for monitoring CO2 and respiration rate of all hospital patients. CO2 measurements are indicated for patients weighing over 5kg (11lbs). The S/5 FM Monitor and N-F(C)(REC) Extension Module are indicated for use by qualified medical personnel only. The Datex-Ohmeda S/5 PSM module (consisting of E-PSM, E-PSMP and E-INTPSM Modules) and accessories is intended for monitoring hemodynamic parameters of hospitalized patients. The Datex-Ohmeda S/5 PSM module (consisting of E-PSM, E-PSMP and E-INTPSM Modules) and accessories are indicated for monitoring of hemodynamic parameters of all hospital patients. The hemodynamic parameters of the module comprise ECG (including ST-segment and arrhythmia), Impedance respiration, NIBP, Temperature, SpO2 (including monitoring during conditions of clinical patient motion), and invasive blood pressure. Impedance Respiration measurement is indicated for patients ages 3 and up. The NIBP measurement is indicated for patients who weigh 5 kg (11 lbs.) and up. The device is indicated for use by qualified medical personnel only. NOTE: E-INTPSM Module is not in use with the S/5 FM.

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 IPX1 - degree of protection against harmful ingress of water. In accordance with EU Medical Device Directive The Datex-Ohmeda S/5 FM 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. • Class A equipment is suitable for use in all establishments other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

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.”

Trademarks S/5, D-lite, D-lite+, Pedi-lite, Pedi-lite+, Mini D-fend, D-fend, D-fend+, MemCard, ComBar, ComWheel, EarSat, FingerSat, FlexSat, PatientO2, Entropy and Patient Spirometry are trademarks of GE Healthcare Finland Oy. Datex, Ohmeda, and OxyTip+ are trademarks of GE Healthcare Finland Oy and Datex-Ohmeda, Inc. All other product and company names are property of their respective owners.

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

Datex-Ohmeda S/5 FM Technical Reference Manual, Order code: M1181261 3rd edition Part I, General Service Guide Document No.

Updated

Description

M1187317-009

Introduction, System description, Installation, Interfacing, Functional check, General troubleshooting

1

M1187318-003

Planned Maintenance Instructions

2

Part II, Product Service Guide Document No.

Updated

Description

M1187329-003

S/5 FM Service Menu

1

M1187335-004

Frame for FM

2

M1215098-002

Patient Side Module, E-PSM, E-PSMP

3

M1187338-003

S/5 Extension Module for FM, N-FC, N-FCREC, N-FREC

4

M1187342-004

S/5 Remote Controller, K-REMCO, K-CREMCO

5

M1187344-003

Device Interfacing Solution, N-DIS

6

M1187346-007

S/5 FM Spare Parts

7

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Table of contents

Table of contents Table of contents

i

Table of figures

iii

List of tables

iv

About this manual

1

1

3

Introduction 1.1

1.2

2

System description 2.1 2.2 2.3 2.4 2.5 2.6

3

1.0.1 Compatibility... 3 Symbols... 4 1.1.1 Symbols on transport packaging... 4 1.1.2 Symbols on equipment... 4 1.1.3 Equipment safety symbols... 5 1.1.4 Other symbols... 6 Safety... 9 1.2.1 Safety precautions... 9 1.2.2 ESD precautionary procedures... 13 Introduction... 14 Bus structure... 14 Distributed processing... 15 Module communication... 15 Software loading... 16 Parameter modules... 17

System installation 3.1 3.2 3.3

3.4 3.5 3.6

14

18

Unpacking instructions... 18 Choosing location... 18 Mounting the S/5 FM... 18 3.3.1 E-PSM(P) Mounting Accessories... 18 3.3.2 Monitor connections... 20 3.3.3 Connection to mains... 22 3.3.4 Connection to Network... 22 3.3.5 Connection to Wireless Network... 22 3.3.6 Inserting and removing the parameter modules... 23 3.3.7 Downloading Monitor Software F-FM(W)-00... 23 3.3.8 Downloading Monitor Software, F-FM(W)-01... 24 3.3.9 Performing Factory Reset... 25 3.3.10 Installing the Datex-Ohmeda Wireless Network Upgrade, U-FMW (F-FM-00)... 25 3.3.11 Installing the Datex-Ohmeda Wireless Network Service Option, N-FMWS (F-FM-00)... 27 3.3.12 Installing the S/5 Wireless Network Upgrade, U-FMW-01... 28 Remote Controller, K-CREMCO... 31 Visual indicators... 31 Troubleshooting... 31 i Document no. M1187317-009

Datex-Ohmeda S/5 FM

4

Interfacing 4.1

4.2

4.3 4.4

5

Interfacing external bedside devices via Device Interfacing Solutions, N-DISxxx... 32 4.1.1 Device Interfacing Solution components... 33 4.1.2 Connections... 33 4.1.3 Mounting... 34 4.1.4 Selecting the external device... 34 4.1.5 Functional check... 35 4.1.6 Selecting the parameter data source... 35 Interfacing printer... 36 4.2.1 Setting S/5 FM interface for printers... 36 4.2.2 Connection to serial printers... 36 4.2.3 Connection to parallel printers... 36 4.2.4 Installing the Serial-to-Parallel Converter... 36 4.2.5 Connection to printer... 37 Interfacing computer... 37 Output signals... 38 4.4.1 Digital outputs... 38 4.4.2 Analog outputs... 38

Functional check 5.1 5.2 5.3

6

32

40

Recommended tools... 41 Visual inspection... 42 Functional inspection... 42 5.3.1 General... 42 5.3.2 Display... 43 5.3.3 Keyboard(s)... 43 5.3.4 Frame unit... 43 5.3.5 Extension Module with CO2 measurement... 43 5.3.6 Multiparameter Hemodynamic Modules... 44 5.3.7 Data Card and Menu Card function... 45 5.3.8 Recorder... 45 5.3.9 Network connection... 45 5.3.10 Wireless Network Option... 45 5.3.11 Device Interfacing Solution, N-DISxxx... 45 5.3.12 General... 46

General troubleshooting

47

Appendix A:

Functional check form, Datex-Ohmeda S/5 FM

A-1

Appendix B:

ElectroMagnetic Compatibility

B-1

Appendix C:

Channel Mask Selections for S/5 FM

C-1

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Table of figures

Table of figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Figure 8 Figure 9 Figure 10 Figure 11

S/5 FM with N-FCREC (1) and E-PSM (2) modules ... 3 General bus structure of S/5 FM ...14 Principle of UPI section operation ...15 General structure of parameter modules with patient isolation...17 E-PSM(P) mounting accessories ...19 S/5 FM front panel ...20 Rear panel connections ...21 Connection cables and LED indicators ...33 An example of interfacing external devices with Device Interfacing Solution...34 Connecting S/5 FM monitor to printer, converter model PI130-R2 ...37 S/5 FM general troubleshooting flowchart ...47

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List of tables Table 1 Table 2 Table 3 Table 4 Table 5 Table 6 Table 7 Table 8 Table 9

DIS modules and interfaced devices... 32 NET ID connector, X8 on Multi I/O adapter ... 38 Defib & IABP sync connector, X5 ... 38 Patient simulators’ compatibility with each hemodynamic module... 41 Adapter cables for hemodynamic patient simulators ... 42 Guidance and manufacturer’s declaration – electromagnetic emissions... B-1 Guidance and manufacturer’s declaration – electromagnetic immunity... B-2 Guidance and manufacturer’s declaration – electromagnetic immunity... B-3 Recommended separation distances between portable and mobile RF communications equipment and the S/5 FM ... B-4

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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 FM.

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 M1181261. The manual includes Technical Reference Manual Slots and every slot has an individual document number.

•

Part I gives the reader an overview of the S/5 FM. 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 FM, 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.

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.

Ordering manuals A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the cover page of the manual.

Related documentation S/5 FM Monitor For instructions for daily use including cleaning and daily maintenance, clinical aspects and basic methods of measurement see: S/5 FM Monitor, User’s Guide S/5 FM Monitor, 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.

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Conventions used To help you find and interpret information easily, the manual uses consistent text formats:



Sign the check form after performing the procedure.

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.

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Introduction

1

Introduction The Datex-Ohmeda S/5 FM is a modular multiparameter patient monitor. The monitor is especially designed for monitoring in intensive care units. It can also be used during transportation within the hospital. 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 wireless networking. 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.

1 2

Figure 1

S/5 FM with N-FCREC (1) and E-PSM (2) modules

1.0.1 Compatibility S/5 FM is compatible with:

S/5 L-FICU04/A

S/5 L-FICU06/A

Patient Side Modules, S/5 E-PSM and E-PSMP

x

x

Extension Module S/5 F-FC

x

x

Extension Modules, S/5 N-FCREC, and N-FREC

x

x

Device Interfacing Solution S/5 N-DISxxx, rev. 01 and later

x

x

S/5 Network and iCentral

x

x

Wireless LAN is available with WLAN option F-FMW

x

x

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1.1 Symbols 1.1.1 Symbols on transport packaging 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.

1.1.2 Symbols on equipment

This battery contains lead and can be recycled.

Pb Dangerous voltage.

Pb/Cd/Hg

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The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements (Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the technical or service manual, or equipment instructions. Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http://www.gehealthcare.com/euen/weee-recycling/index.html

Introduction

1.1.3 Equipment safety symbols -

Attention, consult accompanying documents.

-

When displayed next to the HR value, indicates that the pacer is set on R.

-

On the N-FC(REC) module indicates that the airway gases should be calibrated every 6 months in normal use and every two months in continuous use to ensure that the measurement accuracy remains within specifications.

-

On the E-PSM(P) module:

WARNING

-

On the rear or bottom panel:

WARNING WARNING WARNING WARNING

CAUTION CAUTION

-

Protection against cardiac defibrillator discharge is due in part to the accessories for pulse oximetry (SpO2), temperature (T) and invasive pressure (P) measurement. Electric shock hazard. Do not open the cover or the back. Refer servicing to qualified service personnel. Do not touch the monitor during defibrillation procedure. Disconnect from the power supply before servicing. When using the monitor with mounting attached, make sure that the mounting is manufacturer approved. For continued protection against fire hazard, replace the fuse only with one of the same type and rating. Lithium battery on the CPU board. Dispose of the battery in accordance with local environmental and waste disposal regulations.

On top of the monitor beside the battery cover:

WARNING

Use manufacturer recommended batteries only. Dispose of the batteries in accordance with local environmental and waste disposal regulations.

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.

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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.

1.1.4 Other symbols 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 Submenu. Selecting an alternative marked with this symbol in a menu opens a new menu.

A B

B

B

B

Battery operation and remaining capacity. The height of the green bar indicates the charging level.

Battery (A) charging (white bar)

Battery (A) failure

Both batteries have failed

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Introduction

B

Battery (A) is missing

In the front panel: mains or external DC power. (External DC power for future use.)

The monitor is connected to the Datex-Ohmeda Network (Local Area Network, LAN). The monitor is connected to the Datex-Ohmeda S/5 Network (Wireless Local Area Network, WLAN). Data Card (green) 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.

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Date of manufacturer

Manufacturer name and address

Does not contain Latex.

Do not immerse the sensor in liquids. IPX class:

Degree of protection against harmful ingress of water as detailed in the IEC 60529: IPX0 IPX1 IPX2 IPX3 IPX4 IPX7 IPX8

- 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.

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Introduction

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. 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 an intact and undamaged power cord. Replace the power cord if it is cracked, frayed, broken or otherwise damaged.

• • • •

All system devices must be connected to the same power supply circuit.

•

When detaching modules, be careful not to drop them. Always support with one hand while pulling out with the other.

•

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.

Do not use the power cord delivered with this product for any other product or purpose. Use only hospital-grade grounded power outlets and power cord. Do not remove the grounding pin from the power plug.

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.

Installation

• •

Do not incinerate a battery or store at high temperatures as it will explode.

•

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.

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.

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• •

Do not use the monitor in high electromagnetic fields (for example, during MRI.)

•

If you accidentally drop the monitor, modules or frames, have them checked by authorized service personnel prior to clinical use.

• • •

To avoid explosion hazard, do not use the monitor in presence of flammable anesthetics.

A printer or computer must be supplied from an additional transformer providing at least basic isolation (isolating or separating transformer).

Do not touch the patient, table, instruments, modules or the monitor during defibrillation. Other transmitting radio devices using the same radio frequency band (Industrial Scientific and Medical 2.45 GHz band) may degrade or disturb the wireless network communication.

External connection

•

Do not connect any external devices to the monitor other than those specified.

Explosion hazard

•

To avoid explosion hazard do not use the monitor in the presence of flammable anesthetics.

•

Do not incinerate a battery or store at high temperatures as it will explode.

Patient safety

•

Do not perform any testing or maintenance on the monitor while it is being used on a patient.

•

PACEMAKER PATIENTS: The impedance respiration measurement may cause rate changes in Minute Ventilation Rate Responsive Pacemakers. In this case, set the pacemaker rate responsive mode off or turn the monitor impedance respiration measurement off.

• •

Never install the monitor so that it is above the patient.

•

Operation of the monitor outside the specified values may cause inaccurate results.

When using the monitor with mounting attached, make sure that the mounting is manufacturer approved.

Autoclaving and sterilizing

•

Do not autoclave any part of the system with steam or sterilize with ethylene oxide.

Cleaning and service

•

Only trained personnel with proper tools and test equipment should perform the tests and repairs described in this manual. Unauthorized service may void the monitor warranty.

•

Always unplug the monitor before cleaning or service. After cleaning or service ensure that every part of the monitor is dry before reconnecting it to the power supply.

•

Do not touch any exposed wire or conductive surface while any cover is removed and the monitor is energized. The voltages present can cause injury or death.

•

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”.

•

NOTE! The monitor is always internally powered when the batteries are connected.

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Introduction

•

Electrostatic discharge through the PC boards may damage the components. Before handling PC boards, wear a grounded antistatic wristband. Handle all PC boards by their non-conductive edges and use antistatic containers when transporting them.

• •

Do not break or bypass the patient isolation barrier when testing PC boards.

•

Handle the water trap and its contents as you would any body fluid. Infectious hazard may be present.

•

Do not immerse any part of the device in any liquid, or allow liquid to enter the monitor or modules.

•

If liquid has accidentally entered the system or its parts, disconnect the power cord from the power supply, remove the batteries from the monitor and have the equipment serviced by authorized service personnel.

•

Since calibration gas contains anesthetic agents, always ensure sufficient ventilation of the room during calibration.

Always perform an electrical safety check and a leakage current test on the monitor after service.

Accessories

•

Use only accessories, including mounts, and batteries, and defibrillator-proof cables and invasive pressure transducers approved by GE Healthcare. For a list of approved supplies and accessories, see the “Supplies and Accessories” catalog. Other cables, batteries, transducers and accessories may cause a safety hazard, damage the equipment or the system, result in increased emissions or decreased immunity of the equipment or system or interfere with the measurement. (Protection against cardiac defibrillator discharge is due in part to the accessories for pulse oximetry (SpO2), temperature (T) and invasive pressure (P) measurement.)

•

Single-use products are not designed to be reused. Reuse may cause a risk of cross-contamination, affect the measurement accuracy and/or system performance, or cause a malfunction as a result of the product being physically damaged due to cleaning, disinfection, re-sterilization and/or reuse.

Special components Special components are used in these monitors that are vital to assure reliability and safety. GE Healthcare assumes no responsibility for damage, if replacement components not approved by GE Healthcare are used.

Batteries The Lithium Ion batteries are recyclable. Follow your local recycling guidelines. Refresh the batteries completely every six months. To replace the batteries safely, please refer to the service instructions in this manual.

•

Do not short-circuit the battery terminals, this may produce a very high current, which will damage the battery.

•

Do not dispose of the battery into open flame, nor put the battery near fire, as it may explode.

• •

Do not dismantle the battery. After replacing a battery, always make sure to close the battery compartment by sliding the lid back to the right until it clicks.

See also section “Symbols”.

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Storage and transport Do not store or transport the monitor outside the specified temperature, pressure and humidity ranges: Temperature Atmospheric pressure Relative humidity

-20...+60 °C/-4...140 °F 670...1060 hPa/500...800 mmHg/670...1060 mbar 10...90% noncondensing

Disposal

•

Dispose of the whole device, parts of it and its packing material and manuals in accordance with local environmental and waste disposal regulations.

•

Dispose the calibration gas container in accordance with local environmental and waste disposal regulations.

Cautions CAUTION

A CAUTION indicates a condition that may lead to equipment damage or malfunction. Installation

• •

Leave space for air circulation to prevent the monitor from overheating.

•

Turn off the power before making any rear panel connections.

Before connecting the power cord to the power supply, check that the local voltage and frequency correspond with the rating stated on the device plate.

Before use

•

Allow two minutes for warm-up and note any error messages or deviations from normal operation.

Fuse replacement Replace a fuse only with one of the same type and rating.

Cleaning and service

•

Do not use hypochlorite-, acetone-, phenol- or ammonia -based cleaners, abrasive material or harsh chemicals as they may damage the surfaces of the device.

•

Do not use abrasive cleaning compounds, instruments, brushes or rough-surface materials.

•

Do not apply pressurized air to any outlet or tubing connected to the monitor.

Special components

•

Lithium battery on the CPU board. Dispose of the battery in accordance with local environmental and waste disposal regulations.

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