Tyco 1928L User Manual

Touchmonitor User Guide
1928L 19” LCD Desktop Touchmonitor 5000 Series
User Guide
1928L 19” LCD Desktop Touchmonitor
Revision C
P/N E116103
Copyright © 2007 Tyco Electronics Corporation. All Rights Reserved.
Disclaimer
The information in this document is subject to change without notice. Elo TouchSystems makes no representations or warranties with respect to the contents hereof, and specifically disclaims any implied warranties of merchantability or fitness for a particular purpose. Elo TouchSystems reserves the right to revise this publication and to make changes from time to time in the content hereof without obligation of Elo TouchSystems to notify any person of such revisions or changes.
Trademark Acknowledgments
Elo Touchsystems AccuTouch and IntelliTouch are trademarks of Tyco Electronics Corporation. Other product names mentioned herein may be trademarks or registered trademarks of their re­spective companies.
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 can be connected to ET1928L 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 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)
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. Operating 0oC to 40oC
Storage / Transportation -20oC to +60oC
Humidity (non-condensing)
Operating 30% to 70% Storage / Transportation 10% to 90%
Altitude Operating 1060hpa.
Storage / Transportation 0 to 40,000ft(12,192m)
Equivalent to 1013-303 hP.A (14.7 to 4.4 psia)
For full Product Specifications refer to Appendix C
vii
European Standards and Classifications
Standards: EN 60601-1-2: 2001
The EMC limits and test methods are referred to the following standards: Emission: Immunity CISPR 11: 2003+A1:2004 IEC 61000-4-2: 2001 AS/NZS CISPR 11:2004 IEC 61000-4-3: 2002+A1:2002 (Group 1, Class B) IEC 61000-4-4: 2004
IEC 61000-4-5: 2001 EN55011: 1998+A1: 1999+ IEC 61000-4-6: 2003+A1:2004 A2: 2002, (Group 1, Class B) IEC 61000-4-8: 2001
IEC 61000-4-11: 2004 IEC 61000-3-2: 2000, (Refer to note * below) IEC 61000-3-3; 1995+A1: 2001
Note *: The power consumption of EUT is 50.474W, which is less than 75W and no limits apply. Therefore it is deemed to comply with IEC 61000-3-2: 2000 without any testing.
viii
Guidance and manufacturer’s declaration-electromagnetic immunity-
for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic emissions
The ET1928L is intended f or use in the electromagnetic environment specified below. The customer or the user of the ET1928L should a ssure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment-guidelines
RF emissions Group 1 The ET1928L uses RF energy only for its internal CISPR 11 function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby electronic equipment.
RF emissions The ET1928L is suitable for use in all establishments, CISPR 11
Harmonics emissions network that supplies buildings used for domestic IEC 61000-3-2
Voltage fluctuations/ flicker emissions Complies 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 ET1928L is intended for use in the electromagnetic environment specified below. The customer or the user of the ET1928L should assure that it is used in such an environment.
Immunity test IEC 60601 Compliance level Electromagnetic environment­test level guidelines
Electrostatic ± 6 kV contact ± 6 kV contact Floors should be wood, concrete or discharge(ESD) ± 8 kV air ± 8 kV air ceramic tile. If floors are covered with IEC 61000-4-2 synthetic material, the relative humidity
should be at least 30%.
Electrical Fast ± 2 kV for power ± 2 kV for power Mains power quality should be that of a tra nsient/burst supply lines supply lines typical commerical or hospital
environment.
IEC 61000-4-4 ± 1 kV for input/output ± 1 kV for input/output
lines lines
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 earth typical commerical or hospital
environment.
Voltage dips, short <5% U
T <5% UT Mains power quality be that of a
interruption and (>95% dip in UT) (>95% dip in UT) typical commerical or hospital voltage variations for 0.5 cycle for 0.5 cycle environment. If the user of the ET1928L on power supply requires continued operation during power input lines 40% U
T 40% UT mains interruptions, it is recommended that
(60% dip in UT) (60 % dip in UT) the ET1928L be powered from an
IEC 61000-4-11 for 5 cycles for 5 cycles uninterruptible power supply or a battery.
T 70% UT
70% U (30% dip in UT) (30% dip in UT) for 25 cycles for 25 cycles
T <5% UT
<5% U (>95% dip in UT) (>95% dip in UT) for 25 cycles for 25 cycles
Power frequency 3 A/m 3A/m Power frequency magnetic fields (50/60 Hz) should be at levels characteristic of a magnetic field typical 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 ET1928L is intended f or use in the electromagnetic environment specified below. The user of the ET1928L should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance Electromagnetic environment-guidelines
level
Portable a nd mobile RF communications equi pment should be used no closer to a ny part of theET1928L, including cables, than the recommended separation dista nce calculated from the equation applicable to the frequency of the tra nsmitter.
Recommended separation distance
Conducted RF 3 Vrms 3 Vrms d=1.2 P
Radiated RF 3 V/m 3 Vrms d=1.2 P 80MHz to 800 MHz IEC 61000-4-3 80 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 manufa cturer 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 and 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 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 filed strength in the location in which the ET1928L is used exceeds the applicable RF compliance level above, the ET1928L should be observed to verify normal operation. If abnormal performance is observed, a dditional measures may be necessary, such as reorienting or relocating the ET1928L.
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 ET1928L
for all EQUIPMENT AND SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between portable
and mobile RF communications equipment and the ET1928L
The ET1928L is intended for use in a n electromagnetic environment in which ra di ated RF disturba nces are controlled. The customer or the user of the ET1928L can help prevent electromagnetic interference by maintaining a mini­mum dista nce between portable and mobile RF communications (equipment) and the ET1928L as recommended below according to the maxi mum output power of the communications equipment.
Separation distance according to frequency of transmitter
Rated maximum output 150 kHz to 80 MHz 80MHz to 800 MHz 800 MHz to 2.5 GHz
power of transmitter
W d=1.2 Pd=1.2 Pd=2.3 P
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 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) 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 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
Chapter 1
INTRODUCTION 1
Product Description ................................................1
LCD Display Performance Features .......................2
19 inch TFT LCD Display Panel ......................2
External Medical Grade Power Supply............2
Chapter 2
INSTALLATION AND SETUP 3
Unpacking Your Touchmonitor ...............................3
Product Overview ........................................... 4
Main Unit ......................................................... 4
Back Unit .........................................................4
Side View.........................................................4
Base Bottom View ...........................................5
Kensington
Touch Interface Connection....................................6
Step 1 Connecting the Video Cable ................6
Step 2 Connecting the Serial/USB Cable........7
Step 3 Connecting the Speaker Cable ............8
Step 4 Connecting the Power Cable ...............9
Mounting the Display ............................................10
Rear Mounting Using the VESA Interface ............11
VESA Mounting Options .......................................11
Optimizing the LCD Display..................................12
Installing the Touch Driver Software.....................12
TM
Lock ...........................................5
Power Display & Power Saving ............................17
General Power Saving Mode ........................17
Display Angle.................................................17
Chapter 4
TROUBLESHOOTING 19
Solutions to Common Problems ................................. 19
Appendix A
NATIVE RESOLUTION 21
Appendix B
TOUCHMONITOR SAFETY 23
Care and Handling of Your Touchmonitor ...................24
Appendix C
TECHNICAL SPECIFICATIONS 25
Display Modes .............................................................25
Touchmonitor Specifications........................................26
Power Supply Cord Selection ......................................27
North America.......................................................27
Cord selection for other than North America ........28
AccuTouch (resistive) Touchscreen Specifications .....30
IntelliTouch (acoustic) Touchscreen Specifications .....31
Appendix D
CONTACT ELO 33
Contact Elo .............................................................33
REGULATORY INFORMATION 35
WARRANTY 37
INDEX 39
Chapter 3
OPERATION 13
About Touchmonitor Adjustments................................13
Side Panel Controls.......................................14
Controls and Adjustment ......................................15
OSD Menu Functions ....................................15
OSD Locking and Unlocking Feature ............15
OSD Control Options.....................................16
Product Description
C H A P T E R
1
INTRODUCTION
The 1928L is a medical display designed to present information to the operator and the customer. The 1928L is available in serial and USB(combo) touch interface as well as non-touch. The 1928L functionally consists of a 19” LCD main display with a touchscreen. The main display element is a 19” diagonal SXGA resolution (1280 x 1024) LCD display. The display consists of an LCD display and touchscreen. The 1928L is powered by 12 VDC from an external medical grade power source.
1-1
LCD Display Performance Features
19” TFT LCD Display Panel
Display format 1280 x 1024 Display area 376.32 mm (H) x 301.056 mm (V) Pixel pitch 0.294 mm (H) x 0.294 mm (V) Contrast Ratio 1300:1( typical) Brightness
LCD 300 cd/m2 (typical) AccuTouch 246 cd/m2 (typical)
IntelliTouch 276 cd/m2(typical) Accutouch transmission 82% (typical) Intellitouch transmission 92% (typical) Response time Tr = 15 msec / Tf = 5 msec typical;
12 ms gray to gray response Display color 16.7 million colors Typical vertical viewing angle 89 deg (down) / 89 deg ( up) Typical horizontal viewing angle 89 deg (left) / 89 deg (right)
External Medical Grade Power Supply
The 1928L is powered by an external medical grade universal input AC power source. Power supply:
AC power: Input voltage 100 -240 VAC, 1.0A
Input frequency 50/60 Hz
DC output Voltage/Current: 12 VDC/4.0A
Load regulation: ±5% Max.
Line regulation: ±1% Max.
1-2 Elo Touchmonitor User Guide
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 cable USB cable
Serial Cable European power cable Power cable US/Canada
Elo QuickStart
CD
Software
DVI Cable CD and Quick Install Guide Power adaptor
2-3
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