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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, TouchT ools and V uPoint are trademarks of Elo and its Af filiates. Windows is a trad emark of Microsoft
Corporation.
• 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.
Guidance and manufacturer’s declaration-electromagnetic immunity
for all
EQUIPMENT AND SYSTEMS
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
RF emissions
CISPR 11
Harmonics
emissions
IEC 61000-3-2
Voltage
fluctuations/flicker
emissions
IEC 61000-3-3
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.
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.
Guidance and manufacturer’s declaration-electromagnetic immunity –
for all ME EQUIPMENT AND ME SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic immunity
The 1929LM Touchmonitor for Healthcare Applications isintendedforuseintheelectromagnetic
environmentspecifiedbelow.Thecustomer, ortheuser of the 1929LM Touchmonitor for Healthcare
Applications,
should assure that it is used in such an environment.
ImmunityTest
Electrostatic
discharge (ESD)
61000-4-2
IEC
Electrical fast
tr
ansient/burst
61000-4-4
IEC
Surge
61000-4-5
IEC
Voltagedips,short
interruption
voltage
and
variations
on power supply
inputlines
IEC
61000-4-11
IEC
60601
test level
± 6
kVcontact kVair
± 8
±2 kV for power
supply lines
± 1
kV for
input/output lines
1kVline(s)to
±
line(s)
2kVline(s)to
±
earth
U
<5%
(>95%
T
dipinU
for 0.5 cycle
40%
U
T
(60%
dipinU
for 5 cycles
U
70%
(30%
T
dipinU
for 25 cycles
U
<5%
(>95%
T
dipinU
for 250 cycles
Compl
± 6 kV
kVair
± 8
iance level
contact
Electromagnetic environment – guidance
Floors should be wood, concrete or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
± 2 kV for power
supply lines
± 1 kV for
Mains power quality should be that of a
typical commercial or hospital environment.
input/output Lines
± 1 kV line(s) to
line(s)
Mainspowerqualityshouldbe thatofa
typical commercial or hospital environment.
± 2 kV line(s) to
earth
U
<5%
(>95%
)
T
T
dipinU
)
T
for 0.5 cycle
U
40%
)
T
(60
T
%dipinU
)
T
for 5 cycles
U
70%
)
T
(30%
T
dipinU
)
T
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.
for 25 cycles
U
<5%
(>95%
)
T
T
dipinU
)
T
for 250 cycles
PowerFrequency
(50/60
Magnetic
Hz)
Field
A/m 3 A/m Power frequency magnetic fields should be
3
at levels characteristic of a typical location in
a typical commercial or hospital
environment.
IEC 61000-4-8
NOTE UT is the a.c. mains voltage prior to application of the test level.
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 1929LM Touchmonitor for Healthcare Applications is intended for use in theelectromagnetic
environment
should assure that it is used in such an environment.
specifiedbelow. Theuserofthe 1929LM Touchmonitor for Healthcare Applications
Immunity Test IEC 60601 Test
Level
Conducted RF
Radiated RF
IEC 61000-4-3
3 Vrms
3 V/m
80 MHz to 2.5
GHz
Compliance
Level
3 V
3 V/m
Electromagnetic Environment-Guidelines
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 survey
be less than the compliance level in each frequency
b
range
.
a
, should
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.
and m o b i l e RF co mmu n ica t ion s e q u ip men t and t h e 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)
150 kHz to 80 MHz
Separation distance according to frequency of transmitter
m
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.