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or tra nslated 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 specifically disclaims any
implied warranties of merchanta bility or fitne ss 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
AccuT ouch, CarrollT ouch, Elo T ouchSyste ms, IntelliT ouch, Tyco Electronics a nd TE (logo) are
tra demarks of the Tyco Electronics group of companie s and its licensors. Windows is a trademark
of the Microsoft group of companies. Other product na mes mentioned here in 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 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 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 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 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 fluorescent 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.)
iv
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 ca n be connected to ET2400LM
in Patient Environment. The use of ACCESSOR Y equi pment not complying with the
equivalent safety requirements of this equipment may lead to a reduced safety of the re sulting
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 har
monized 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 specified, 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.
v
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 reason
ably expected to result in significant 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.
Definitions:
“ 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.
vi
Classification
With respect to electrical shock, fire in accordance with UL60601-1 and CAN/CSA C22.2 No.
60601-1
This monitor is a Class I (GROUNDED) DEVICE.
These displays are classified NO APPLIED PARTS EQUIPMENT.
Protection against harmful ingress of water:
INGRESS PROTECTION (IPX1) (for monitor only)
This monitor 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
Temp.Operating0oC to 40oC
Storage / Transportation-20oC to +60oC
Humidity (non-condensing)
Operating20% to 80%
Storage / Transportation10% to 90%
AltitudeOperating0 to 3,000M
Storage / Transportation0 to 12,192M
For full Product Specifications refer to Appendix C
vii
European Standards and Classifications
Standards: EN 60601-1-2: 2001+A1:2004
The EMC limits and test methods are referred to the following standards:
Emission:Immunity
CISPR 11: 2003+A1:2004IEC 61000-4-2: 2008
AS/NZS CISPR CISPR22: 2006IEC 61000-4-3: 2006+A1:2007
(Group 1, Class B)IEC 61000-4-4: 2004
Guidance and manufacturer’s declaration-electromagnetic immunity-
for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic emissions
The ET2400LM is intended for use in the electromagnetic environment specified below. The customer or the user
of the ET2400LM should assure that it is used in such an environment.
RF emissionsGroup 1The ET2400LM uses RF energy only for its internal
CISPR 11function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby
electronic equipment.
RF emissionsThe ET2400LM is suitable for use in all e sta blishments,
CISPR 11
Harmonics emissionsnetwork that supplies buildings used for domestic
IEC 61000-3-2
Voltage fluctuations/
flicker emissionsComplies
IEC 61000-3-3
Class B
including domestic establishments and those directly
connected to the public low-voltage power supply
Not applicable
purposes.
ix
Guidance and manufacturer’s declaration-electromagnetic immunity-
for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic immunity
The ET2400LM is intended for use in the electromagnetic environment specified below. The customer or the user
of the ET2400LM should assure that it is used in such an environment.
Electrostatic± 6 kV contact± 6 kV contactFloors should be wood, concrete or
discharge(ESD)± 8 kV air± 8 kV airceramic tile. If floors are covered with
IEC 61000-4-2synthetic material, the relative humidity
should be at least 30%.
Electrical Fast± 2 kV for power± 2 kV for powerMains power quality should be that of a
tra nsient/burstsupply linessupply linestypical commerical or hospital
environment.
IEC 61000-4-4± 1 kV for input/output± 1 kV for input/output
lineslines
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 earthtypical commerical or hospital
environment.
Voltage dips, short<5% U
T<5% UTMains power quality be that of a
interruption and(>95% dip in UT)(>95% dip in UT)typical commerical or hospital
voltage variationsfor 0.5 cyclefor 0.5 cycleenvironment. If the user of the ET2400LM
on power supplyrequires continued operation during power
input lines40% U
T40% UTmains interruptions, it is recommended that
(60% dip in UT)(60 % dip in UT)the ET2400LM be powered from an
IEC 61000-4-11for 5 cyclesfor 5 cyclesuninterruptible power supply or a battery.
T70% UT
70% U
(30% dip in UT)(30% dip in UT)
for 25 cyclesfor 25 cycles
T<5% UT
<5% U
(>95% dip in UT)(>95% dip in UT)
for 25 cyclesfor 25 cycles
Power frequency3 A/m3A/mPower frequency magnetic fields
(50/60 Hz)should be at levels characteristic of a
magnetic fieldtypical location in a typical commerical
or hospital environment.
IEC 61000-4-8
NOTE U
T is the a.c. mains voltage prior to application of the test level.
x
Guidance and manufacturer’s declaration-electromagnetic immunity-
for all EQUIPMENT AND SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration-electromagnetic immunity
The ET2400LM is intended for use in the electromagnetic environment specified below. The user of the ET2400LM
should assure that it is used in such an environment.
Immunity testIEC 60601 test level ComplianceElectromagnetic environment-guidelines
level
Portable a nd mobile RF communications equi pment
should be used no closer to any part of the
ET2400LM, including cables, tha n the recommended
separationdistance calculated from the equation ap
plicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF3 Vrms 3 Vrmsd=1.2 P
Radiated RF3 V/m 3 Vrmsd=1.2 P 80MHz to 800 MHz
IEC 61000-4-380 MHz to 2.5 GHz
d=2.3 P 800 NHz to 2.5GHz
where P is the maximum output power rating of
the tra nsmitter in watts (W) according to the
transmitter manufacturer and d is the recommended
separation distance in metres(m)
Filed strengths from fixed RF tra nsmitters, as
determined by a n electromagnetic site survey
3
,
should be less than the compliance level in each
frequency ra nge4.
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 situation. Electromagnetic propagation is af fected by a bsorption an d
reflection from structures, objects and people.
3.
Filed 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 broadca st 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 filed strength in the location in which the ET2400LM is used exceeds the
applica ble RF compli ance level a bove, the ET2400LM should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as reorienting or relocating the ET2400LM.
4.
Over the frequency ra nge 150 kHz to 80 MHz, field strengths should be less than 3 Vrms.
xi
Recommended separation distance between portable and mobile
RF communications equipment and the ET2400LM
for all EQUIPMENT AND SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between portable
and mobile RF communications equipment and the ET2400LM
The ET2400LM is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the ET2400LM ca n help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications (equipment) and the ET2400LM as
recommended below according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
Rated maximum output150 kHz to 80 MHz80MHz to 800 MHz800 MHz to 2.5 GHz
power of transmitter
Wd=1.2 Pd=1.2 Pd=2.3 P
0.010.120.120.23
0.10.370.370.74
11.21.22.3
103.73.77.4
100121223
For transmitters rated at a maximum output power not listed above, the recommended separation distance d 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) a ccording 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 af fected by absorption
a nd reflection from structures, objects and people.
xii
Table of Contents
Warnings and Cautions................................................. iv
Warning ................................................................. iv
Caution ................................................................... v
Caution-Life Support .....................................................vi
Classification ................................................................ vii
European Standards and Classifications
Standards ............................................................ viii
Power Display & Power Saving..............................23
General Power Saving Mode...........................23
Controls and Adjustment ........................................21
OSD Menu Functions.......................................21
OSD Locking a nd Unlocking Feature ................ 21
OSD Control Options .......................................22
Product Description
C H A P T E R
1
INTRODUCTION
The 2400LM is a medical display designed to present information to the operator and the customer .
The 2400LM is available in serial and USB(combo) touch interface as well as non-touch. The
2400LM functionally consists of a 24” LCD main display with a touchscreen. The main display
element is a 24” diagonal WUXGA re solution (1920 x 1200) LCD display . The display consists of an
LCD display and touchscreen. The 2400LM is powered by 12 VDC from an external medical grade
power source.
1-1
LCD Display Perf ormance Fe atures
24” TFT LCD Display Panel
Display format1920x 1200
Display area518.4 mm (H) x 324.0 mm (V)
Pixel pitch0.270 mm (H) x 0.270 mm (V)
Contrast Ratio1000:1( typical)
Brightness
L C D300 cd/m2 (typical)
IntelliTouch270 cd/m2(typical)
V ertical V iewing AngleTypical V ertical V iewing Angle: 80deg(looking down)
/80 deg(lookingup) @ CR>=10
Horizontal Viewing AngleTypical Vertical V iewing Angle: 80deg(looking left)
/80 deg(looking right) @ CR>=10
External Medical Grade Power Supply
The 2400LM is powered by a n external medical grade universal input AC power source.
Power supply:
•AC power: Input voltage 100 -240 VAC, 1.27A
•Input frequency 50/60 Hz
•DC output Voltage/Current: 12 VDC/6.5A
•Load regulation: ±5% Max.
•Line regulation: ±1% Max.
1-2
C H A P T E R
2
INSTALLATION AND SETUP
This chapter discusses how to install your LCD touchmonitor and how to install Elo TouchSystems
driver software.
Unpacking Your Touchmonitor
Check that the following items are present and in good condition:
LCD monitor VGA cableUSB cableSerial cable
Power cable European Power cable UK Power cable US/Canada Power cable Japanese(European model only) (European model only) (North American model only) (Japan model only)
Elo QuickStart
CD
Software
CD and Quick Install GuidePower ada ptor DV I ca bl eAudio cable
2-3
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