Elo TouchSystems 2400LM Manuel utilisateur

Touchmonitor User Guide

2400LM 24” LCD Desktop Touchmonitor

EloTouchSystems

24” LCD

Touchmonitor

User Guide

Revision D

SW601252

Elo

ouchSystems

1-800-ELOTOUCH

www.elotouch.com

iii

No part of this publication may be reproduced, transmitted, transcribed, stored in a retrieval

system, or translated into any language or computer language, in any form or by any means,

including, but not limited to, electronic, magnetic, optical, chemical, manual, or otherwise

without prior written permission of Tyco Electronics.

Disclaimer

The information in this document is subject to change without notice. Tyco Electronics

Corporation and its Afffiliates in the TE Touch Solutions business unit in the TE

Connectivity Ltd. family of companies (collectively “TE”) makes no representations or

warranties with respect to the contents herein, and specificallydisclaims any implied warranties

of merchantability or fitnessfor a particular purpose. TE reserves the right to revise this

publication and to make changes from time to time in the content hereof without obligation of

TE to notify any person of such revisions or changes.

TrademarkAcknowledgments

AccuTouch, Elo (logo), Elo TouchSystems, IntelliTouch, TE Connectivity, TE connectivity

(logo) and TE (logo) are trademarks of the TE Connectivity Ltd. family of companies.

Windows is a trademark of the Microsoft group of companies. Other product names mentioned

herein may be trademarks or registered trademarks of their respective companies. Tyco

Electronics claims no interest in trademarks other than its own.

Warnings and Cautions

Warning

• Danger - Explosion hazard. Do not use in the presence of flammableanesthetics, and other

flammablematerials.

• To prevent fire or shock hazards, do not immerse the unit in water or expose it to rain or

moisture.

• Do not use the unit with an extension cord receptacle or other outlets unless the prongs of

the power cord can be fully inserted.

• RISK OF ELECTRICAL SHOCK - DO NOT OPEN. To reduce the risk of electrical shock,

DO NOT remove the back of the equipment or open the enclosure. No user-serviceable

parts are inside. Refer servicing to qualifiedfieldservice engineers only.

• Uninsulated voltage within the unit may have sufficientmagnitude to cause electrical

shock. Avoid contact with any part inside the unit.

• This device complies with all applicable electromagnetic emission and immunity standards

for medical device equipment. This device is designed to not cause harmful interference,

and to accept any interference received, including interference that may cause undesired

operation. The performance of this device is limited to the emission and immunity

standards that have been applied. Other device which are not designed to withstand

emission levels as specified in the medical device standards may be susceptible to

interference from this device.

Subjecting the device to conditions beyond the rated performance capabilities may result in

emissions in excess of the standard. If it is determined that this device produces

electromagnetic or other interference it must be disconnected from power until the cause of

the problem has been determined and resolved. If it is determined that this device is

functioning improperly due to electromagnetic and other interference it must be

disconnected from power until the cause of the problem has been determined and resolved.

• Elo TouchSystems recommends that after its useful life (or after sustaining unrepairable

damage), customers dispose of the touchmonitor and its power supply in an

environmentally sound manner. Acceptable methods include the reuse of parts or whole

products and the recycling of products, components, and materials. Please consult and obey

national state, and local laws and ordinances governing the safe disposal of electronic

equipment.

Note that the fluorescent lamps inside this product contain mercury and must be recycled or

disposed of according to local, state, or national laws. For more information, contact the

Electronic Industries Alliance at www.eiae.org.

This product consists of devices that may contain mercury, which must be recycled or disposed

of in accordance with local, state, or federal laws. (Within this system, the backlight lamps in

the monitor display contain mercury.)

Caution

• Power cord is used as a disconnection device. To de-energize equipment, disconnect the

power cord.

• This unit must follow the national requirement and local state laws to dispose unit.

• Before connecting the cables to your Elo touchmonitor, make sure all components are

powered OFF.

Only approved components complying with IEC60601-1 series can be connected to

ET2400LM in Patient Environment. The use of ACCESSORY equipment not complying

with the equivalent safety requirements of this equipment may lead to a reduced safety of

the resulting system. Consideration relating to the choices of accessory equipment should

include:·

Use of accessory in the patient environment.·Evidence that the safety

certificationof the accessory has been performed in accordance to the appropriate IEC

60601-1 and/or IEC 60601-1-1 harmonized national standard.

• For continued safety -

- This unit only complies to the above standards if used with a medical grade power cord.

-A medical grade power supply, such as the one specified,is required for use in a medical

application.

Note:

• This symbol alerts the user to important information concerning the operation and

maintenance of this unit, which should be read carefully to avoid problems.

• This symbol means DC Current.

• This symbol means ON/OFF stand-by switch.

CAUTION-Life Support

Care must be taken when this touchmonitor is a critical component of a life support system or

device. In case of failure of this touchmonitor, appropriate redundant systems should be

incorporated into the system or device to prevent injury to the user or patient.

The following should be an integral part of the safety design of a life support system or device

using this touchmonitor for a critical function.

• An alternate interface or fail-safe must be available should the touchscreen fail to operate.

• The touchscreen interface must not be the only means of control of a critical function.

• An alternate video display should be incorporated into the safety design if used to monitor a

critical function.

• The internal speakers of this touchscreen monitor must not be the sole method of warning

of a critical function.

Critical functions are:

1. Life support devices or systems are devices or systems which, (a) are intended for surgical

implant into the body, or (b) support or sustain life, or (c) whose failure to perform when

properly used in accordance with instructions for use provided in the labeling, can be

reasonably expected to result in significant injury to the user.

2. A critical component is any component of a life support device or system whose failure to

perform can be reasonably expected to cause the failure of the life support device or system,

or to affect its safety or effectiveness.

Definitions:

“ PATIENT ENVIRONMENT”

any environment in which intentional or unintentional contact can occur between a PATIENT

and parts of the ME EQUIPMENT or ME SYSTEM or between a PATIENT and other persons

touching parts of the ME EQUIPMENT or ME SYSTEM.

Classification

With respect to electrical shock, fire in accordance with UL60601-1 and CAN/CSA C22.2 No.

60601-1

This monitor is a Class I (GROUNDED) DEVICE.

These displays are classifiedNOAPPLIED PARTS EQUIPMENT.

Protection against harmful ingress of water:

INGRESS PROTECTION (IPX1) (for monitor only)

This monitor shall be classified as ORDINARY EQUIPMENT, not intended or evaluated for

use in the presence of flammableanesthetic mixture with air, oxygen, or nitrous oxide.

Mode of Operation: CONTINUOUS OPERATION.

Environmental conditions for transport and storage

o o

Temp. Operating 0 C to 40 C

o o

Storage / Transportation -20 C to +60 C

Humidity (non-condensing)

Operating 20% to 80%

Storage / Transportation 10% to 90%

Altitude Operating 0 to 3,000M

Storage / Transportation 0 to 12,192M

For full Product Specificationsrefer to Appendix C

vii

European Standards and Classifications

Standards: EN 60601-1-2: 2001+A1:2004

The EMC limits and test methods are referred to the following standards:

Emission: Immunity

CISPR 11: 2003+A1:2004 IEC 61000-4-2: 2008

AS/NZS CISPR CISPR22: 2006 IEC 61000-4-3: 2006+A1:2007

(Group 1, Class B) IEC 61000-4-4: 2004

IEC 61000-4-5: 2005

EN55011: 2007+A1: 2007 IEC 61000-4-6: 2008

(Group 1, Class B) IEC 61000-4-8: 2009

IEC 61000-4-11: 2004

IEC 61000-3-2: 2006,

(Refer to note * below)

IEC 61000-3-3: 2008

viii

Guidance and manufacturer’s

declaration-electromagnetic

immunity-

for all

EQUIPMENT

AND SYSTEMS

Guidance and manufacturer’s

declaration-elect

oma

netic

emissions

The ET2400LM is intended for use in the electromagnetic environment specified below. The customer or the

user of the ET2400LM should assure that it is used in such an environment.

Emissions test Compliance Electromagnetic environment-guidelines

RF emissions

CISPR 11

Group 1 The ET2400LM uses RF energy only for its internal

function. Therefore, its RF emissions are very low and

are not likely to cause any interference in nearby

electronic equipment.

RF emissions

CISPR 11

Class B

Harmonics emissions

IEC 61000-3-2

Not applicable

Voltage fluctuations/

flickeremissions

IEC 61000-3-3

Complies

The ET2400LM is suitable for use in all establishments,

including domestic establishments and those directly

connected to the public low-voltage power supply

network that supplies buildings used for domestic

purposes.

Guidance and manufacturer’s

declaration-electromagnetic

immunity-

for all

EQUIPMENT

AND SYSTEMS

Guidance and manufacturer’s

declaration-electromagnetic

immunity

The ET2400LM is intended for use in the electromagnetic environment specified below. The customer or the

user of the ET2400LM should assure that it is used in such an environment.

Immunity test

test level IEC 60601 Compliance level Electromagneticenvironment-

guidelines

Electrostatic

discharge(ESD)

IEC 61000-4-2

± 6 kV contact

± 8 kV air

± 6 kV contact

± 8 kV air

Floors should be wood, concrete or

ceramic tile. If floorsare covered with

synthetic material, the relative humidity

should be at least 30%.

Electrical Fast

transient/burst

IEC 61000-4-4

± 2 kV for power

supply lines

± 1 kV for input/output

lines

± 2 kV for power

supply lines

± 1 kV for input/output

lines

Mains power quality should be that of a

typical commerical or hospital

environment.

Surge

IEC 61000-4-5

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

Mains power quality should be that of a

typical commerical or hospital

environment.

Voltage dips, short

interruption and

voltage variations

on power supply

input lines

IEC 61000-4-11

<5% UT

(>95% dip in UT)

for 0.5 cycle

40% UT

(60% dip in UT)

for 5 cycles

70% UT

(30% dip in UT)

for 25 cycles

<5% UT

(>95% dip in UT)

for 25 cycles

<5% UT

(>95% dip in UT)

for 0.5 cycle

40% UT

(60 % dip in UT)

for 5 cycles

70% UT

(30% dip in UT)

for 25 cycles

<5% UT

(>95% dip in UT)

for 25 cycles

Mains power quality be that of a typical

commerical or hospital environment. If the

user of the ET2400LM requires continued

operation during power mains

interruptions, it is recommended

that the ET2400LM be powered from an

uninterruptible power supply or a battery.

Power frequency

(50/60 Hz)

magnetic field

IEC 61000-4-8

3 A/m 3A/m Power frequency magnetic

fields

should

be at levels characteristic of a typical

location in a typical commerical or

hospital environment.

NOTE UT is the a.c. mains voltage prior to application of the test level.

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