S5 Anesthesia Monitor Users Reference Manual Jan 2003

Intended purpose (Indications for use) The Datex-Ohmeda S/5 Anesthesia Monitor with L-ANE03 or L-ANE03A software is intended for multiparameter patient monitoring with optional patient care documentation. The S/5 Anesthesia Monitor with L-ANE03 and L-ANE03A 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 Anesthesia Monitor with L-ANE03 and L-ANE03A 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 Anesthesia Monitor with L-ANE03 and L-ANE03A software is also indicated for documenting patient care related information. The S/5 Anesthesia Monitor with L-ANE03 and L-ANE03A software is indicated for use by qualified medical personnel only.

Classifications In accordance with IEC 60601-1 CLASS I 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 IPX0 - the degree of protection against harmful ingress of water. In accordance with EU Medical Device Directive The Datex-Ohmeda S/5 Anesthesia Monitor is classified as IIb.

Responsibility of the manufacturer Datex-Ohmeda Division, Instrumentarium Corporation 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 Datex-Ohmeda.

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the electrical installation of the monitor room complies with appropriate requirements.

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the equipment is used in accordance with the "User's Guide."

Trademarks Datex®, Ohmeda®, and other trademarks S/5, D-lite, D-lite+, Pedi-lite, Pedi-lite+, D-fend, D-fend+, TruTrak®+, OxyTip+, MemCard, ComWheel, ComBar, EarSat, FingerSat, FlexSat, PatientO2, Patient Spirometry and Tonometrics are property of Instrumentarium Corp. or its subsidiaries. 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.

End User License Agreement THIS DOCUMENT IS A LEGAL AGREEMENT BETWEEN YOU, THE "PURCHASER," AND DATEX-OHMEDA (“D-O”). IF YOU DO NOT AGREE TO THE TERMS OF THIS AGREEMENT, PROMPTLY RETURN THE ENTIRE PACKAGE, INCLUDING ALL ACCESSORIES, IN THEIR ORIGINAL PACKAGE, WITH YOUR SALES RECEIPT TO D-O FOR A FULL REFUND. 1. Grant of License. In consideration of payment of the license fee, which is part of the price paid for this product, D-O grants to Purchaser a nonexclusive, nontransferable license, without right to sublicense, to use the copy of the incorporated software/firmware, and documentation in connection with Purchaser's use of the product for their labeled purpose and only when the instrument is used with authorized accessories and sensors. D-O reserves all rights not expressly granted to Purchaser. 2. Ownership of Software/Firmware. Title to, ownership of, and all rights and interests in, any software and/or firmware and the documentation, and all copies thereof, remain at all times vested in D-O or its partners, and they do not pass to Purchaser. 3. Assignment. Purchaser shall not assign or transfer this License, in whole or in part, by operation of law or otherwise, without D-O's prior written consent. Any attempt without such consent, to assign any rights, duties or obligations hereunder shall be void. You may not transfer, assign, rent, lease, sell, or otherwise dispose of the software/firmware or the products on a temporary basis. 4. Copy Restrictions. The software/firmware and the accompanying written materials are copyrighted. Unauthorized copying of the software, including software that has been modified, merged, or included with other software, or other written materials is expressly forbidden. You may be held legally responsible for any copyright infringement that is caused or incurred by your failure to abide by the terms of this license. 5. Use Restriction. As the Purchaser, you may physically transfer the products from one location to another provided that the software/firmware is not copied. You may not electronically transfer the software/firmware from the products to any other device. You may not disclose, publish, translate, release or distribute copies of the software/firmware to others. You may not modify, adapt, translate, reverse engineer, decompile, disassemble, or create derivative works based on the software/firmware, unless specifically permitted by local law. Your license to the software is not valid for use with any unauthorized data acquisition device. 6. Applicable Law and Jurisdiction This Software License is construed, governed by and interpreted in accordance with the laws of Finland, excluding the UN Convention on Contracts for the International Sale of Goods and the parties hereto irrevocably submit to the exclusive jurisdiction of the lower court of Helsinki, Finland.

Warranty This Product is sold by Datex-Ohmeda under the warranty set forth in the following paragraphs. Such warranty is extended only with respect to the purchase of this Product directly from Datex-Ohmeda or DatexOhmeda’s Authorized Dealers as new merchandise and is extended to the Buyer thereof, other than for the purpose of resale. For a period of twelve (12) months from the date of original delivery to Buyer, this Product, other than expandable parts, is warranted against functional defects in materials and workmanship and to conform to the description of the Product contained in this manual and accompanying labels and/or inserts, provided that the same is properly operated under the conditions of normal use, that regular periodic maintenance and service is performed and that the replacements and repairs are made in accordance with the instructions provided, using genuine parts and performed by a trained person. The foregoing warranty shall not apply if the Product has been repaired by anyone other than Datex-Ohmeda or otherwise than in accordance with written instructions provided by Datex-Ohmeda, or altered by anyone other than DatexOhmeda, or if the Product has been subject to abuse, misuse, negligence, or accident. Datex-Ohmeda’s sole and exclusive obligation and Buyer’s sole and exclusive remedy under the above warranty is limited to repairing or replacing, free of change, at Datex-Ohmeda’s option, a Product, which is telephonically reported to the nearest Datex-Ohmeda office or Datex-Ohmeda’s Authorized Dealers office and which, if so advised by Datex-Ohmeda, is thereafter returned with a statement of observed deficiency, not later than seven (7) days after the expiration date of the applicable warranty, to the Datex-Ohmeda office or Datex-Ohmeda’s Authorized Dealers office during normal business hours, transportation charges prepaid, and which, upon Datex-Ohmeda’s examination, is found not to conform to the above warranty. DatexOhmeda shall not be otherwise liable for any damages including but not limited to incidental damages, consequential damages, or special damages. There are no express or implied warranties, which extend beyond the warranty hereinabove set forth. DatexOhmeda makes no warranty of merchantability or fitness for particular purpose with respect to the product or parts thereof.

Table of contents

Table of contents ABOUT THIS MANUAL 1.

SAFETY

2.

SYSTEM DESCRIPTION

3.

MONITORING BASICS

4.

INTERFACING

5.

ALARMS

6.

MONITOR SETUP

7.

TRENDS AND SNAPSHOTS

8.

PATIENT DATA MANAGEMENT

9.

RECORDING AND PRINTING

10. CLEANING AND CARE 11. TROUBLESHOOTING 12. ECG 13. PULSE OXIMETRY 14. TEMPERATURE 15. INVASIVE BLOOD PRESSURE 16. IMPEDANCE RESPIRATION 17. CARDIAC OUTPUT 18. MIXED VENOUS OXYGEN SATURATION 19. NON-INVASIVE BLOOD PRESSURE 20. AIRWAY GASES 21. PATIENT SPIROMETRY 22. GAS EXCHANGE 23. TONOMETRY 24. NEUROMUSCULAR TRANSMISSION 25. EEG AND EP 26. BISPECTRAL INDEX 27. ENTROPY 28. INDEX 29. SUPPLIES AND ACCESSORIES CATALOG

1

Table of contents

Table of contents About this manual

1

General ...1 Conventions used ...1 Additional information ...2 Installation and service...2 Clinical application...2 References ...3

About this manual

About this manual General This User’s Reference Manual describes the functions offered by the Datex-Ohmeda S/5 Anesthesia Monitor running the software license L-ANE03 or L-ANE03A. As the monitor setup may vary, some menus, displays and functions described may not be available in the monitor you are using. NOTE: Before using your Datex-Ohmeda S/5 Anesthesia Monitor, please read the User’s Guide Part I and Part II or this manual thoroughly. The User’s Reference Manual gives you more specific information about the clinical and technical aspects. Pay special attention to WARNING and CAUTION statements appearing throughout the manual. The new user of the Datex-Ohmeda S/5 Anesthesia Monitor should begin with sections "Safety," "System description" and "Monitoring basics." These sections describe the system and the basic operation of the monitor. The measurement sections describe the measurement technique, setup and how to adjust display and menus for patient monitoring and special views. The "Monitor setup" section gives instructions about setting up the system and making changes in the default settings.

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

WARNING

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Names of the hard keys on the Remote Controller, Command Bar and modules are written in the following way: Others.

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Menu items are written in bold italic typeface: Lab Data.

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Menu access is described from top to bottom. For example, the selection of the Monitor Setup hard key, the Screen Setup menu item and the Waveform Fields menu item would be shown as Monitor Setup - Screen Setup - Waveform Fields.

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Messages (alarm messages, informative messages) displayed on the screen are written inside single quotes: ‘Learning’.

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When referring to different sections in this manual, section names are written in italic typeface and enclosed in double quotes: “Cleaning and care”.

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When referring to other manuals, the manual names and section names are written in italic typeface and enclosed in double quotes: “Datex-Ohmeda S/5 Critical Care Monitor User’s Reference Manual: Cleaning and care”.

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Warnings are written in bold typeface, for example:

Connect only one patient to a monitor at a time.

1

Datex-Ohmeda S/5 Anesthesia Monitor

-

CAUTION

Cautions are written in the following way:

Turn off the power before making any rear panel connections The following symbols are also used to distinguish procedures:

ECG

Press the menu key described.

Turn the ComWheel.

Push the ComWheel.

Additional information For more information about the Datex-Ohmeda S/5 Central, S/5 Arrhythmia Workstation and anesthesia record keeping solution, see the "User’s Reference Manuals" for these products. Software options and default settings are described in the "Default Configuration Worksheet" delivered separately with each monitor. Datex-Ohmeda accessories are described in the Datex-Ohmeda "Supplies and accessories" catalog.

Installation and service A separate "Technical Reference Manual" describes installation, interfacing, connectors, service, maintenance and reparation procedures of the S/5 Anesthesia Monitor. Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the "Technical Reference Manual." Service and reparations are allowed by authorized service personnel only. Section "Cleaning and care" describes cleaning and daily maintenance procedures.

Clinical application Detailed information on clinical applications can be found in several Datex-Ohmeda publications. Datex-Ohmeda produces application guides about patient spirometry, CO2 monitoring, PCWP, cardiac output, ST segment analysis, impedance respiration, etc.

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About this manual

References 1.

ANSI/AAMI EC11:1991 Diagnostic electrocardiographic devices

2.

ANSI/AAMI EC13:2002 Cardiac monitors, heart rate meters, and alarms

3.

ANSI/AAMI EC57:1998 Testing and reporting performance results of cardiac rhythm and ST segment measurement algorithms

4.

ANSI/AAMI SP10:2002 Manual, electronic or automated sphygmomanometers.

5.

EN1060-1:1995 Non-invasive sphygmomanometers –Part 1: General requirements.

6.

EN1060-3:1997 Non-invasive sphygmomanometers –Part 3: Supplementary requirements for electromechanical blood pressure measuring systems.

7.

IEC 60601-2-25:1993 + Amd 1:1999 Medical electrical equipment Part 2-25: Particular requirements for the safety of electrocardiographs

8.

IEC 60601-2-27:1994 Medical electrical equipment Part 2: Particular requirements for the safety of electrocardiographic monitoring equipment

9.

IEC 60601-2-30:1999 Medical electrical equipment Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment.

10.

IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems.

11.

IEC 60601-1-2:2001 Medical electrical equipment Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests

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Table of contents

Table of contents 1 Safety

1–1

Safety precautions... 1–1 Warnings... 1–1 Cautions ... 1–2 ESD precautionary procedures ... 1–2 ESD precautionary procedure training ... 1–2 Points to note ... 1–3 Disposal... 1–3

Safety

1 Safety Safety precautions The following list contains all the general warnings and cautions you should know before starting to use the system. Warnings and cautions specific to parts of the system can be found in the relevant section.

Warnings WARNING

A WARNING indicates a situation in which the user or the patient may be in danger of injury or death. •

To avoid explosion hazard, do not use the Datex-Ohmeda S/5 Anesthesia Monitor in presence of flammable anesthetics. The monitor measures only non-flammable anesthetics.

•

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 by DatexOhmeda.

•

Connect only one patient to a monitor at a time.

•

Use only hospital-grade grounded power outlets and power cord.

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Some equipment malfunctions may not generate a monitor alarm. Always keep the patient under close surveillance.

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

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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.

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Do not touch the patient, table, instruments or the monitor during defibrillation.

•

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. See "ESD precautionary procedures" later in this section for details.

•

Use only cables, transducers and accessories approved by Datex-Ohmeda. Other cables, transducers and accessories may damage the system, result in increased emissions or decreased immunity of the system or interfere with the measurement. Single-use accessories are not designed to be re-used. Re-use may cause a risk of contamination and affect the measurement accuracy.

•

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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If liquid has accidentally entered the equipment, disconnect the power cord from the power supply and have the equipment serviced by authorized service personnel.

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If the unit fails to respond as described, do not use the monitor until tested and repaired by authorized service personnel.

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The system is intended for use by qualified medical personnel only. 1–1

Datex-Ohmeda S/5 Anesthesia Monitor

Cautions CAUTION

A CAUTION indicates a situation in which the unit or the devices connected to it may be damaged. •

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 on the rear panel of the monitor.

•

Turn off the power before making any rear panel connections.

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

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Do not store or use the monitor outside the temperature and humidity ranges specified in the "System description: Specifications" section of this manual.

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Do not subject memory cards to excessive heat, bending or magnetic fields.

ESD precautionary procedures •

To avoid electrostatic charges to build up, it is recommended to store, maintain and use the equipment at a relative humidity of 30% or greater. Floors should be covered by ESD dissipative carpets or similar. Non-synthetic clothing should be used when working with the component.

•

To prevent applying a possible electrostatic discharge to the ESD sensitive parts of the equipment, one should touch the metallic frame of the component or to a large metal object located close to the equipment. When working with the equipment and specifically when the ESD sensitive parts of the equipment may be touched, a grounded wrist strap intended for use with ESD sensitive equipment should be worn. Refer documentation provided with the wrist straps for details of proper use.

ESD precautionary procedure training It is recommended that all potential users receive an explanation of the ESD warning symbol and training in ESD precautionary procedures. The minimum content of an ESD precautionary procedure training should include an introduction to the physics of electrostatic charge, the voltage levels that can occur in normal practice and the damage that can be done to electronic components if they are touched by and operator who is electrostatically charged. Further, an explanation should be given of methods to prevent build-up of electrostatic charge and how and why to discharge one’s body to earth or to the frame of the equipment or bond oneself by means of a wrist strap to the equipment or the earth prior to making a connection.

1–2

Safety

Points to note •

Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the "Technical Reference Manual."

•

Portable and mobile RF communications equipment can affect the medical electrical equipment.

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The allowed Datex-Ohmeda cables, transducers and accessories for the system are listed in the Supplies and accessories catalog.

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The equipment is suitable for use in the presence of electrosurgery. Please notice the possible limitations in the parameter sections.

•

Dispose of the whole device and parts of it in accordance with local environmental and waste disposal regulation.

Disposal

1–3

Table of contents

Table of contents 2 System description

2–1

Principles of functions... 2–1 System introduction... 2–2 Central Unit ... 2–3 Rear of the Central Unit... 2–4 Extension frame ... 2–5 Displays ... 2–6 15” video display, D-VMC15... 2–6 15” LCD display, D-LCC15 ... 2–7 10” LCD display, D-LCC10A... 2–8 19” LCD display, D-LCC19 ... 2–9 17” video display, D-VHC17 ... 2–10 Module overview... 2–11 Measurement modules... 2–11 Measurement modules, cont... 2–12 Compact airway modules, Single-width Airway Module ... 2–12 Other modules ... 2–12 Avoiding identical modules ... 2–13 General module description ... 2–14 Keyboards ... 2–16 Command Bar ... 2–16 Anesthesia record keeping solution keyboard ... 2–16 Remote Controller ... 2–17 Symbols and abbreviations ... 2–18 Equipment safety symbols ... 2–18 Other symbols ... 2–19 15” video display symbols ... 2–20 15” LCD display symbols ... 2–21 17” video display symbols ... 2–21 Abbreviations... 2–23 Specifications... 2–35 Power supply... 2–35 Environmental conditions ... 2–35 Hemodynamic Modules M-NE12STPR, M-NESTPR, M-NE12TPR, M-NETPR, M-NE12STR, M-NESTR, M-ESTPR, M-ETPR, M-ESTR; M-P, M-PP, M-PT; M-NIBP ... 2–35 Cardiac Output Modules, M-COP and M-COPSv... 2–36 Compact Airway Modules, M-C, M-CO, M-COV, M-CAiO, M-CAiOV, M-CAiOVX... 2–36 Compact Airway Modules, M-C, M-CO, M-COV, M-CAiO, M-CAiOV, M-CAiOVX (cont.)... 2–37 Single-width Airway Module, M-miniC... 2–37 Nellcor Compatible Saturation Module, M-NSAT ... 2–38 Datex-Ohmeda Compatible Saturation Module, M-OSAT ... 2–38 Neuromuscular Transmission Module, M-NMT ... 2–38 Tonometry module, M-TONO ... 2–38 EEG module, M-EEG ... 2–38 BIS Module, M-BIS ... 2–39 Entropy Module, M-ENTROPY ... 2–39

System description

2 System description Principles of functions The S/5 Anesthesia Monitor is a modular multiparameter patient monitor. The monitor is especially designed for anesthesia monitoring. The true 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 and monitor networking. External devices can be interfaced to the monitor with interface modules.

2–1

Datex-Ohmeda S/5 Anesthesia Monitor

System introduction The Datex-Ohmeda S/5 Anesthesia Monitor may consist of the elements shown below.

3 4 2

1

5

9

10

7 8

6

11 12

Figure 2-1

Datex-Ohmeda S/5 Anesthesia Monitor

(1)

15” video display, D-VMC15

(2)

15” LCD display, D-LCC15

(3)

10” LCD display, D-LCC10A

(4)

19" LCD display, D-LCC19

(5)

17” video display, D-VHC17; wall-mountable only

(6)

Printer

(7)

Extension Frame, F-EXT4

(8)

Extension Module, M-EXT

(9)

Remote Controller, K-REMCO

(10)

Central Unit, F-CU8 (also called 8-Module Frame)

(11)

Measurement modules

(12)

Anesthesia record keeping solution keyboard

NOTE: After transferring or reinstalling the monitor, always check that it is properly connected and securely attached. NOTE: The allowed Datex-Ohmeda cables, transducers and accessories for the monitor are listed in the Supplies and accessories catalog.

2–2

System description

WARNING

Connect only one patient to the monitor at a time.

WARNING

A secondary display and printer must be supplied from an additional transformer providing at least basic isolation (isolating or separating transformer). Without an appropriate transformer the leakage current of the secondary display can be too high.

WARNING

Never install the monitor or the displays so that they are above the patient.

WARNING

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 by Datex-Ohmeda.

Central Unit The Central Unit (8-Module Frame) houses up to eight single-width modules. It accepts patient data from the modules and formats it for the display. Using the connector in the rear, data and waveforms are sent to the display or other peripherals.

1

Figure 2-2

2

Central Unit

(1)

Insertion guide

(2)

Module connector

2–3

Datex-Ohmeda S/5 Anesthesia Monitor

Rear of the Central Unit

8

9

10

1

11

13

16

2 21 !

18 20

3

4

6

7 5

Figure 2-3

12

19 14

15

17

Rear of the Central Unit

(1)

Receptacle for power cord and fuses

(2)

Power outlet for displays

(3)

Equipotential connector

(4)

Service reset button

(5)

Network board, B-UPI4NET

(6)

Parallel printer port

(7)

RS-232 output

(8)

Direct ECG output

(9)

Network connector

(10)

Identification plug

(11)

Connector for the S/5 Device Interfacing Solution, DIS

(12)

CPU Board, B-CPU5, which contains the software and a PC card connector. The cover plate can be moved when upgrading the software with a PC card.

(13)

Connector for future use

(14)

Display controller board, B-DISP

(15)

Display connector

(16)

Connector for Command Bar and Remote Controller

(17)

Board for anesthesia record keeping solution

(18)

Connector for anesthesia record keeping solution keyboard

2–4

System description

(19)

Interface Board, B-INT

(20)

Serial communication connector

(21)

Module bus connector

Your Central Unit may not have all these boards and the boards may be in different places. With the L-ANE03 or L-ANE03A software license and display board B-DISP (rev. 01) also a third display controller board is possible. If a third B-DISP is used, one of the other boards, for example B-INT, must be removed. The installation and connections are more thoroughly explained in the "Technical Reference Manual."

Extension frame The Extension Frame, F-EXT4, provides four additional module places and flexibility for monitor setup. The frame can be placed beside the Central Unit or moved closer to the patient, for example, attached to the IV pole. Thus the frame can be used as an invasive pressure ‘station’ equipped with invasive pressure measuring modules. The zeroing is easy when the dome stopcock and zeroing keys are near to each other. The modules are used in the same way as in the Central Unit, for example, the module keys function directly. NOTE: Leave free space for the fan filter on the rear panel. NOTE: Use only one Extension Frame in one Central Unit. NOTE: The following modules cannot be used in the Extension Frame: Recorder Module M-REC, Memory Module M-MEM, Interface Module M-INT, or Compact Airway Modules M-Cxxx.

Figure 2-4

Extension frame with extension mount

The monitor end of the cable is plugged as any module into the Central Unit. For installation instructions, see the "Technical Reference Manual." 2–5

Datex-Ohmeda S/5 Anesthesia Monitor

Displays The displays show up to eight (8) waveforms, real-time data and trends. The detachable Command Bar or fixed command board is used to make adjustments in the display and monitored parameters, silence the alarms and reset the monitor to default settings. One S/5 Anesthesia Monitor may have one, two or three independently configurable displays. This means that each display can show different views. Each of the independently configurable displays may have a slave display connected to it. A slave screen displays the same view as the independently configurable one.

CAUTION

The displays must only be used together with the original type of power adapter.

CAUTION

The LCD display is fragile. Ensure that the LCD display is not placed near a heat source or exposed to mechanical shocks, pressure, moisture, or direct sunlight.

15” video display, D-VMC15 With the 15" video display, D-VMC15, the desired information and Command Bar can be brought conveniently near to the patient.

1

2 3

Figure 2-5

4

5

15” video display, D-VMC15

(1)

Video display, D-VMC15

(2)

Command Bar (detachable)

(3)

Command Bar keys

(4)

ComWheel

(5)

ON/STBY switch of the monitor

To use the display, you need a Display Controller Board, B-DISP. For details about changing the screen resolution, see section "Monitor setup: Changing monitor installation settings."

CAUTION

To prevent any liquid from entering the display casing, do not tilt the display more than ±20°.

2–6