Elo TouchSystems 1929LM User Manual

Elo Touch Solutions

1929LM Touchmonitor

USER MANUAL

SW200158 Rev A

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 2 of 31

Copyright © 2014 Elo Touch Solutions, Inc. All Rights Reserved.

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, TouchTools and VuPoint are trademarks of Elo and its Affiliates. Windows is a trademark of Microsoft
Corporation.

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 3 of 31

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 25. 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.

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 4 of 31

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 complying with IEC60601-1 series can be connected to

 For continued safety

the power cord.

are powered OFF.

1929LM touch monitor for Healthcare Applications 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 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 DisclaimerError! Bookmark not defined.:

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.

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 5 of 31

Classification

Temp.

Operating

0°C to 40°C

Storage / Transportation

-20°C to 60°C

Operating

20% to 80%

Storage / Transportation

10% to 90%

Altitude

Operating

0 to 3,048m

Storage / Transportation

0 to 12,192m

With 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)

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

Humidity (non-condensing)

1929LM 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.

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 6 of 31

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

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 7 of 31

Guidance and manufacturer’s declaration-electromagnetic immunity

Guidance and manufacturer’s declaration-electromagnetic emissions

The 1929LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic environment
specified below. The customer or the user of the 1929LM Touchmonitor for Healthcare Applications should
assure that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment-guidelines

RF emissions
CISPR 11

Group 1

The 1929LM 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.

RF emissions
CISPR 11

Class B

The [ME EQUIPMENT or ME SYSTEM] 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.

Harmonics
emissions
IEC 61000-3-2

Class D

Voltage
fluctuations/flicker
emissions
IEC 61000-3-3

Complies

for all

EQUIPMENT AND SYSTEMS

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 8 of 31

Guidance and manufacturer’s declaration-electromagnetic immunity –

Guidance and manufacturer’s declaration-electromagnetic immunityError! Bookmark not

The 1929LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic
environment specified below. The customer, or the user of the 1929LM Touchmonitor for Healthcare

Applications, should assure that it is used in such an environment.

Immunity Test

IEC 60601

test level

Compliance level

Electromagnetic environment – guidance

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 floors are 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 commercial 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 commercial 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 250 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 250 cycles

Mains power quality should be that of a
typical commercial or hospital environment.
If the user of the 1929LM Touchmonitor for
Healthcare Applications requires continued
operation during power mains interruptions,
It is recommended that the 1929LM
Touchmonitor for Healthcare Applications be
powered from an uninterruptible power
supply or a battery.

Power Frequency
(50/60 Hz)
Magnetic Field

IEC 61000-4-8

3 A/m

3 A/m

Power frequency magnetic fields should be
at levels characteristic of a typical location in
a typical commercial or hospital
environment.

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

for all ME EQUIPMENT AND ME SYSTEMS

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 9 of 31

Guidance and manufacturer’s declaration-electromagnetic immunity

Guidance and manufacturer’s declaration-electromagnetic immunity

The 1929LM Touchmonitor for Healthcare Applications is intended for use in the electromagnetic
environment specified below. The user of the 1929LM Touchmonitor for Healthcare Applications
should assure that it is used in such an environment.

Immunity Test

IEC 60601 Test

Level

Compliance
Level

Electromagnetic Environment-Guidelines

Conducted RF
Radiated RF

IEC 61000-4-3

3 Vrms
3 V/m

80 MHz to 2.5
GHz

3 V
3 V/m

Portable and mobile RF communications equipment
should be used no closer to any part of the 1929LM
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 surveya, should
be less than the compliance level in each frequency
rangeb.

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.

a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile

radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically 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 1929LM Touchmonitor for Healthcare
Applications is used exceeds the applicable RF compliance level above, the 1929LM 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 1929LM Touchmonitor for Healthcare Applications.

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

SYSTEMS that are not LIFE-SUPPORTING

for all EQUIPMENT AND

© 2014 Elo Touch Solutions, Inc. All rights reserved.

User Manual – 1929LM

SW200158 Rev A - Page 10 of 31

Recommended separation distances between

portable

and mobile RF communications equipment and the 1929LM Touchmonitor for Healthcare

The 1929LM 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
1929LM Touchmonitor for Healthcare Applications can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications (equipment) and
the 1929LM Touchmonitor for Healthcare Applications as recommended below according to the
maximum output power of the communications equipment.

Rated maximum
output power of
transmitter

(W)

Separation distance according to frequency of transmitter

m

150 kHz to 80 MHz

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 transmitter manufacturer.

NOTE 1: At 80 MHz and 800 MHz, the separation distance for 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.