Elo TouchSystems 1519LM Manual de usuario

Touchmonitor User Guide

1519LM 15.6” LCD Desktop Touchmonitor

1919LM 18.5” LCD Desktop Touchmonitor

Elo TouchSystems

15.6” and 18.5” LCD Touchmonitor

User Guide

Revision A

SW601463

Elo TouchSystems

1-800-ELOTOUCH

www.elotouch.com

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 makes

no representations or warranties with respect to the contents hereof, and specically disclaims

any implied warranties of merchantability or tness for a particular purpose. Tyco

Electronics reserves the right to revise this publication and to make changes from time to time

in the content hereof without obligation of Tyco Electronics to notify any person of such

revisions or changes.

Trademark Acknowledgments

AccuTouch, CarrollTouch, Elo TouchSystems, IntelliTouch, Tyco Electronics and TE (logo) are

trademarks of the Tyco Electronics group of companies and its licensors. 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.

iii

Warnings and Cautions

Warning

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

ammable materials.

• To prevent re 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 qualied eld service engineers only.

• Uninsulated voltage within the unit may have sufcient magnitude 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

specied 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uorescent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

ET1519/ 1919LM 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

certication of 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 specied, 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.

Medical and Healthcare Application Disclaimer: If the Purchaser intends to commercialize, market or

use any product for medical or healthcare applications, it is the sole responsibility of the Purchaser to ensure that

the product is adequate and appropriate for the Purchaser’s intended use and complies with all applicable laws,

regulations, codes and standards including but not limited to the European Union Medical Device Directive, United

States Federal Food, Drug, and Cosmetic Act, regulations of the United States Food and Drug Administration (FDA),

and for obtaining and maintaining any required regulatory approvals including but not limited to any required market

clearances. Tyco Electronics has not sought nor received any rulings from the FDA or any other federal, state, or

local government agency or notied body as to the safety, effectiveness or appropriateness of its product for such

applications. Persons intending to evaluate or use Tyco Electronics’ product for medical or healthcare purposes must

rely on their own medical and legal judgment without any representation on the part of Tyco Electronics.

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 signicant 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.

Denitions:

“ 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.

 Classication

With respect to electrical shock, re in accordance with UL60601-1 and CAN/CSA C22.2

No. 60601-1

This monitor is a Class I (GROUNDED) DEVICE.

These displays are classied NO APPLIED PARTS EQUIPMENT.

Protection against harmful ingress of water:

INGRESS PROTECTION (IPX0)

This monitor shall be classied as ORDINARY EQUIPMENT, not intended or evaluated for

use in the presence of ammable anesthetic mixture with air, oxygen, or nitrous oxide.

Mode of Operation: CONTINUOUS OPERATION.

Environmental conditions for transport and storage

Temp. Operating 0oC to 40oC

Storage / Transportation -20oC to +60oC

Humidity (non-condensing)

Operating 30% to 70%

Storage / Transportation 10% to 90%

Altitude Operating 0 to 3,000m

Storage / Transportation 0 to 40,000ft(12,192m)

Equivalent to 1013-303 hP.A

(14.7 to 4.4 psia)

For full Product Specications refer to Appendix C

vii

E342290

viii

 EuropeanStandardsandClassications

Standards: EN 60601-1-2: 2007

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

Emission: Immunity

CISPR 11: 2009+A1:2010 IEC 61000-4-2: 2008

IEC 61000-4-3: 2006+A1:2007+A2:2010

(Group 1, Class B) IEC 61000-4-4: 2004 + A1:2010

IEC 61000-4-5: 2005

EN55011: 1998+A1: 1999+ IEC 61000-4-6: 2008

A2: 2002, (Group 1, Class B) IEC 61000-4-8: 2009

IEC 61000-4-11: 2004

IEC 61000-3-2: 2005

IEC 61000-3-3; 2008

Guidance and manufacturer’s declaration-electromagnetic emissions

The ET1519/1919LM is intended for use in the electromagnetic environment specied below. The customer or

the user of the ET1519/1919LM should assure that it is used in such an environment.

Emissions test Compliance Electromagnetic environment-guidelines

RF emissions Group 1 The ET1519/1919LM uses RF energy only for its in

CISPR 11 ternal function. Therefore, its RF emissions are very low

and are not likely to cause any interference in nearby

electronic equipment.

RF emissions Class B The ET1519/1919LM is suitabe for use in all

CISPR 11 establishments, including domestic establishments

and those directly connected to the public low-voltage

Harmonics emissions Not applicable power supply network that supplies buildings used

IEC 61000-3-2 for domestic purposes.

Voltage uctuations/ Complies

icker emissions

IEC 61000-3-3

Guidance and manufacturer’s declaration-electromagnetic immunity-

for all EQUIPMENT AND SYSTEMS

Guidance and manufacturer’s declaration-electromagnetic immunity-

for all EQUIPMENT AND SYSTEMS

Guidance and manufacturer’s declaration-electromagnetic immunity

The ET1519/1919LM is intended for use in the electromagnetic environment specied below. The customer or

the user of the ET1519/1919LM should assure that it is used in such an environment.

Immunity test IEC 60601 Compliance level Electromagnetic environment-

test level guidelines

Electrostatic ± 6 kV contact ± 6 kV contact Floors should be wood, concrete or

discharge(ESD) ± 8 kV air ± 8 kV air ceramic tile. If oors are covered with

IEC 61000-4-2 synthetic material, the relative humidity

should be at least 30%.

Electrical Fast ± 2 kV for power ± 2 kV for power Mains power quality should be that of a

transient/burst supply lines supply lines typical commerical or hospital

environment.

IEC 61000-4-4 ± 1 kV for input/output ± 1 kV for input/output

lines lines

Surge ± 1 kV line(s) to line(s) ± 1 kV line(s) to line(s) Mains power quality should be that of a

IEC 61000-4-5 ± 2 kV line(s) to earth ± 2 kV line(s) to earth typical commerical or hospital

environment.

Voltage dips, short <5% UT <5% UT Mains power quality be that of a

interruption and (>95% dip in UT) (>95% dip in UT) typical commerical or hospital

voltage variations for 0.5 cycle for 0.5 cycle environment. If the user of the ET1519/

on power supply 1919LM requires continued operation

input lines 40% UT40% UTduring power mains interruptions, it is

(60% dip in UT)(60 % dip in UT)recommended that the ET1519/1919LM

be powered from an uninterruptible

IEC 61000-4-11 for 5 cycles for 5 cycles power supply or a battery.

70% UT 70% UT

(30% dip in UT) (30% dip in UT)

for 25 cycles for 25 cycles

<5% UT <5% UT

(>95% dip in UT) (>95% dip in UT)

for 25 cycles for 25 cycles

Power frequency 3 A/m 3A/m Power frequency magnetic elds

(50/60 Hz) should be at levels characteristic of a

magnetic eld typical location in a typical commerical

or hospital environment.

IEC 61000-4-8

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

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