Elo TouchSystems 2401LM User Manual

USER MANUAL

Elo Touch Solutions

2401LM Touchmonitor

SW200127 Rev A

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 Elo Touch Solutions, Inc.

Disclaimer

The information in this document is subject to change without notice. Elo Touch Solutions, Inc. and its Affiliates (collectively "Elo") makes no representations or warranties with respect to the contents herein, and specifically disclaims any implied warranties of merchantability or fitness for a particular purpose. Elo reserves the right to revise this publication and to make changes from time to time in the content hereof without obligation of Elo to notify any person of such revisions or changes.

Trademark Acknowledgments

AccuTouch, CarrollTouch, Elo, Elo (logo), Elo Touch, Elo Touch Solutions, Elo TouchSystems, IntelliTouch, iTouch, SecureTouch, Touch Tools and VuPoint are trademarks of Elo and its Af filiates. Windows is a trademark of Microsoft Corporation.

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User Manual 2401LM

Warnings and Cautions

Warning

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

• 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 qualified field service engineers only.

• Uninsulated voltage within the unit may have sufficient magnitude to cause electrical shock.

• Avoid contact with any part inside the unit.

• This device complies with the electromagnetic emission and immunity standards and is limited to the standards that are listed on pages 6 and 26. Other devices 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 Touch Solutions 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.

• To avoid risk of electric shock, this equipment must only be connected to supply mains with protective earth.

This product consists of devices that may contain mercury, which must be recycled or disposed of in accordance with local, state, or federal laws.

SW200127 Rev A - Page 3 of 32

User Manual 2401LM

Caution

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

 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

 Only approved components complyi ng with IEC60 601-1 ser ies ca n b e connecte d to

 For continued safety

the power cord.

are powered OFF.

240 1 L M touch monitor for Healthc ar e Ap p li ca t io ns in Patient Environment. The use of ACCESSORY equi pment not complying with the equivalent safety requirements of this equipment may lea d to a reduced saf ety 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 certification of the accessory has been performed in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1 harmonized national standard.

- 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.

 Please do not touch the patient and the Touchmonitor output connecter at the same

time.

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:

It is the sole responsibility of any person intending to commercialize, market or use any of Elo Touch Solutions, Inc. or its family of companies ("Elo") products for medical or healthcare applications to ensure that such product is adequate and appropriate for the person'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. Elo has not sought nor received any rulings from the FDA or any other federal, state, or local government agency or notified body as to the safety, effectiveness or appropriateness of its product for such applications. Persons intending to evaluate or use Elo's product for medical or healthcare purposes must rely on their own medical and legal judgment without any representation on the part of Elo.

SW200127 Rev A - Page 4 of 32

User Manual 2401LM

Classification

Wit

h respect to electrical shock, fire in accordance with ANSI/AAMI ES60601-1:2005 and

CAN/CSA C22.2 No. 60601-1-08

This Touchmonitor is a Class I (GROUNDED) DEVICE.

These Touchmonitors are classified NO APPLIED PARTS EQUIPMENT.

Protection against harmful ingress of water:

INGRESS PROTECTION (IPX1)

Touchmonitor shall be classified as ORDINARY EQUIPMENT, not intended or evaluated

This for

use in the presence of flammable anesthetic mixture with air, oxygen, or nitrous oxide. Mode of Operation: CONTINUOUS OPERATION. Environmental conditions for transport and storage

Temp. Operating

0°C to 40°C

Storage / Transportation -20°C to 65°C

Humidity (non-condensing)

Operating

Altitude

2401LM Touchmonitor for Healthcare Applications is intended for general use in hospital environment for data collection and display for reference. It shall not be used with life-supporting system.

Storage / Transportation 10% to 90%

Operating

Storage / Transportation 0 to 12,192m

0% to 80%

to 3,000m

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User Manual 2401LM

European Standards and Classifications

Standards: EN 60601-1-2: 2007

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

Emission: Immunity CISPR11:2009+A1:2010 ED. 5.1(Grp I, Class B) IEC61000-4-2:2008 ED.2.0

AS/NZS CISPR 11: 2011, Grp. 1, Class B IEC61000-4-3:2006+A1:2007 +A2:2010ED.3.2 IEC 61000-4-4: 2012 ED.3.0 EN 61000-3-2: 2006 +A1: 2008+A2: 2009, Class D IEC 61000-4-5: 2005 ED.2.0 IEC 61000-3-3: 2008 IEC 610004-6: 2008 ED.3.0 IEC 61000-4-8: 2009 ED.2.0 IEC 61000-4-11: 2004 ED.2.0

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User Manual 2401LM

Guidance and manufacturer’s declaration-electromagnetic immunity

for all

EQUIPMENT AND SYSTEMS

Guidance and manufacturer’s declaration-electromagnetic emissions

The 2401LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic environment specified below. The customer or the user of the 2401LM Touchmonitor for Healthcare Applications should assure that it is used in such an environment.

Emissions test Compliance Electromagnetic environment-guidelines

RF emissions CISPR 11

Harmonics emissions IEC 61000-3-2

Voltage fluctuations/flicker emissions IEC 61000-3-3

Group 1 The 2401LM Touchmonitor for Healthcare Applications 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.

Class A The 2401LM Touchmonitor for Healthcare Applications is suitable

for use in all establishments other than domestic and those directly connected to a low voltage power supply network which supplies buildings used for domestic purposes.

Class D

Complies

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User Manual 2401LM

Guidance and manufacturer’s declaration-electromagnetic immunity

for all EQUIPMENT AND

SYSTEMS

Guidance and manufacturer’s declaration-electromagnetic immunity

The 2401LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic environment specified below. The customer, or the user of the 2401LM Touchmonitor for Healthcare

Applications,

should assure that it is used in such an environment.

Immunity Test Level

Electrostatic

Discharge (ESD)

61000-4-2

IEC

Electrical Fast Tr

ansient/Burst

61000-4-4

IEC

Surge

61000-4-5

IEC

Voltage Dips, Short

Interruption Voltage

and

Variations

on Power Supply

Input Lines

IEC

61000-4-11

60601

IEC

kV contact

± 6

kV air

± 8

± 2 kV for power

supply lines

kV for

± 1

input/output lines

1 kV line(s) to

line(s)

2 kV line(s) to

earth

<5% (>95% for 0.5 cycle

40% (60%

dip in UT)

for 5 cycles

70%

dip in UT)

(30%

for 25 cycles

<5% (>95%

dip in UT)

for 250 cycles

Compl

supply lines

± 1

± 2

<5% (>95% for 0.5 cycle

40% (60 for 5 cycles

70% (30% for 25 cycles

<5% (>95% for 250 cycles

iance Level

± 6 kV

2 kV for power

± 8

contact

kV air

kV for input/output

Lines

± 1 kV line(s) to

line(s)

kV line(s) to earth

dip in UT)

% dip in UT)

dip in UT)

Electromagnetic Environment - Guidelines

Floors tile. If floors are covered with synthetic mater least 30%.

should be wood, concrete or ceramic

ial, the relative humidity should be at

Mains power quality should be that of a

typical commercial or hospital environment.

Mains power quality should be that of a

typical commercial or hospital environment.

Mains power quality should be that of a

typical commercial or hospital environment. If the user of the 2401LM Touchmonitor

for Healthcare Applications requires

continued operation during power mains interruptions, It is recommended that the

2401LM Touchmonitor for Healthcare Applications

uninterruptible power supply or a battery.

be powered from an

Power Frequency (50/60 Magnetic

Hz)

Field

A/m

3 A/m

Power frequency magnetic fields should be at levels char a typical commercial or environment.

IEC 61000-4-8

NOTE UT is the A.C. mains voltage prior to application of the test level.

acteristic of a typical location in

hospital

User Manual 2401LM

SW200127 Rev A - Page 8 of 32

Guidance and manufacturer’s declaration-electromagnetic immunity

SYSTEMS that are not LIFE-SUPPORTING

for all EQUIPMENT AND

Guidance and manufacturer’s declaration-electromagnetic immunity

The 2401LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic environment should assure that it is used in such an environment.

specified below. The user of the 2401LM Touchmonitor for Healthcare Applications

Immunity Test IEC 60601 Test

Level

Conducted RF Radiated RF

IEC 61000-4-3

Vrms V/m

80 MHz to 2.5 GHz

Compliance Level

Vrms

3 Vrms

Electromagnetic Environment-Guidelines

Portable and mobile RF communications equipment should be used no closer to any part of the 2401LM Touchmonitor for Healthcare Applications and should assure that it is used in such an environment, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance

80MHz to 800 MHz

800 MHz to 2.5GHz

where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres(m)

Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey1, should be less than the compliance level in each frequency range2. Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

3. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordl ess) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted th eoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the 2401LM Touchmonitor for Healthcare Applications is used exceeds the applicable RF compliance level above, the 2401LM Touchmonitor for Healthcare Applications should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the 2401LM Touchmonitor for Healthcare Applications.

4. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 Vrms.

User Manual 2401LM

SW200127 Rev A - Page 9 of 32

Recommended separation distances between portable

and mobile RF communications equipment

and the 2401LM Touchmonitor for Healthcare Applications for all EQUIPTMENT AND SYSTEMS that are

not LIFE-SUPPORTING

The 2401LM Touchmonitor for Healthcare Applications is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the 2401LM Touchmonitor for Healthcare Applications can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications (equipment) and the 2401LM Touchmonitor for Healthcare Applications as recommended below according to the maximum output

power of the communications equipment.

Rated Maximum Output Power of Transmitter

(W)

150 kHz to 80 MHz

Separation Distance According to Frequency of Transmitter

80MHz to 800 MHz

800 MHz

to 2.5 GHz

0.01 0.12 0.12 0.23

0.1 0.37 0.37 0.74 1 1.2 1.2 2.3

10 3.7 3.7 7.4

100 12 12 23

For transmitters rated at a maximum output power not listed above, the recommended separation distanced in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the

ansmitter manufacturer.

NOTE 1: NOTE

bsorption and reflection from structures, objects and people.

At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by

User Manual 2401LM

SW200127 Rev A - Page 10 of 32

+ 22 hidden pages

Elo TouchSystems 2401LM User Manual

Specifications and Main Features

Frequently Asked Questions

User Manual

Warnings and Cautions

Classification