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1929LM
User Manual
31 pgs759.44 Kb0

Elo Touch 1929LM User Manual

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Copyright © 2016 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, TouchT ools and V uPoint are trademarks of Elo and its Af filiates. Windows is a trad emark of Microsoft Corporation.
© 2016 Elo Touch Solutions, Inc. All rights reserved.
SW200158 Rev B - Page 2 of 31
User Manual – 1929LM
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.
© 2016 Elo Touch Solutions, Inc. All rights reserved.
SW200158 Rev B - Page 3 of 31
User Manual – 1929LM
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plying wit
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mplying wi
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ipment sh
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portant i
should b t. and-by swi
er:
IEC60601 tions in Pa
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the resulti
uld includ
rtification
e IEC 606
andards if
the one
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pecified, i
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Drug pprovals r receive
or notified
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oses must
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© 20
16 Elo Touch Sol
utions, Inc. All rig
hts reserved.
SW2
User Ma
00158 Rev B -
nual – 1929LM
Page 4 of 31
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ance with
D PARTS
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QUIPMEN
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r use in th
tion: CON conditions
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umidity (no
ainst harmf
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onito
shall
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INUOUS
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ESS PRO
be classifie
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erating
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Transport
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O
erating
Transport
water:
ECTION (
as
ORDIN
anesthetic
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MENT, not
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LM Touch
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Altitude
onitor for
splay for re
Storage /
ealthcare A erence. It
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pplications i
hall not be
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0
s intended used with li
0
to 3,048m
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or general e-supportin
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ent for data
© 20
16 Elo Touch Sol
utions, Inc. All rig
hts reserved.
SW2
User Ma
00158 Rev B -
nual – 1929LM
Page 5 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
© 2016 Elo Touch Solutions, Inc. All rights reserved.
SW200158 Rev B - Page 6 of 31
User Manual – 1929LM
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.
Class D
Complies
© 2016 Elo Touch Solutions, Inc. All rights reserved.
SW200158 Rev B - Page 7 of 31
User Manual – 1929LM
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 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
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
IEC
60601
test level
± 6
kV contact kV air
± 8
± 2 kV for power supply lines
± 1
kV for
input/output lines
1 kV line(s) to
± line(s)
2 kV line(s) to
± earth
U
<5% (>95%
T
dip in U
for 0.5 cycle 40%
U
T
(60%
dip in U
for 5 cycles
U
70% (30%
T
dip in U
for 25 cycles
U
<5% (>95%
T
dip in U
for 250 cycles
Compl
± 6 kV
kV air
± 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)
Mains power quality should be that of a
typical commercial or hospital environment.
± 2 kV line(s) to earth
U
<5% (>95%
)
T
T
dip in U
)
T
for 0.5 cycle
U
40%
)
T
(60
T
% dip in U
)
T
for 5 cycles
U
70%
)
T
(30%
T
dip in U
)
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
dip in U
)
T
for 250 cycles
Power Frequency (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.
© 2016 Elo Touch Solutions, Inc. All rights reserved.
SW200158 Rev B - Page 8 of 31
User Manual – 1929LM
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 the electromagnetic environment should assure that it is used in such an environment.
specified below. The user of the 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.
© 2016 Elo Touch Solutions, Inc. All rights reserved.
User Manual – 1929LM
SW200158 Rev B - Page 9 of 31
Recommended separation distances between
portable
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.
© 2016 Elo Touch Solutions, Inc. All rights reserved.
User Manual – 1929LM
SW200158 Rev B - Page 10 of 31
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