Elo TouchSystems C-Series, 19CX, 22CX User Manual

C-Series Touchcomputer for Healthcare Applications User Guide
C-Series LCD Multi-function Touchcomputer
[19” model shown]
TE Touch Solutions
Applications User Guide
Multi-function Touchcomputer
Revision A
SW601689
1-800-ELOTOUCH (1-800-356-8682)
www.elotouch.com
C-Series Touchcomputer for Healthcare Applications User Guide ii
Copyright © 2011 Tyco Electronics Corporation, a TE Connectivity Ltd. Company.
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 Tyco Electronics Corporation.
Disclaimer
The information in this document is subject to change without notice. Tyco Electronics Corporation and its Afffiliates in the TE Touch Solutions business unit in the TE Connectivity Ltd. family of companies (collectively "TE") 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. TE reserves the right to revise this publication and to make changes from time to time in the content hereof without obligation of TE to notify any person of such revisions or changes.
Trademark Acknowledgments
AccuTouch, Elo TouchSystems, Elo TouchSystems (logo), Elo, IntelliTouch, iTouch, TE Connectivity, TE connectivity (logo) and TE (logo) are trademarks. Windows is a trademark of Microsoft Corporation. Other product names mentioned herein may be trademarks or registered trademarks of their respective companies. TE claims no interest in trademarks other than its own.
C-Series Touchcomputer for Healthcare Applications User Guide iii
Wa rn i ng s an d C au t io ns
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 41 and 45. 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 powe r un t i l t h e c ause of the problem has been determined and resolved.
• TE Touch Solutions recommends that after its useful life (or after sustaining unrepairable damage), customers dispose of the touchcomputer 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
product consists of devices that may contain mercury, which must be recycled or
This disposed of in accordance with local, state, or federal laws. (Within this system, the backlight lamps in the touchcomputer display contain mercury.)
www.eiae.org.
C-Series Touchcomputer for Healthcare Applications 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 touchcomputer, make
sure all components are powered OFF.
Only approved components complying with IEC60601-1 series ca n be
connected to 19CX/ 22 CX Touchcomputer for Healthcare Applications in Patient Environment. The use of ACCESSOR Y 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.
Please do not touch the patient and the touchcomputer 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.
C-Series Touchcomputer for Healthcare Applications v
C-Series Touchcomputer for Healthcare Applications vi
Medical and Healthcare Application Disclaimer:
It is the sole responsibility of any person intending to commercialize, m arket or use any of TE Connectivity Ltd. or its family of companies ("TE") 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. TE 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 TE's product for medical or healthcare purposes must rely on their own medical and legal judgment without any representation on the part of TE.
Classification
With respect to electrical shock, fire in accordance with UL60601-1 and CAN/CSA C22.2 No.
601.1
This touchcomputer is a Class I (GROUNDED) DEVICE.
These touchcomputers are classified NO APPLIED
PARTS EQUIPMENT. Protection against harmful
ingress of water:
INGRESS PROTECTION (IPX1)
This touchcomputer 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 35oC
Storage / Transportation
-30oC to 60oC
Humidity (non-condensing)
Operating 20% to 80%
Storage / Transportation 5% to 95%
Altitude
Operating 0 to 3,00 0m
Storage / Transportation 0 to 12 ,19 2m
19CX/22CX Touchcomputer 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
For full Product Specifications refer to Appendix C
C-Series Touchcomputer for Healthcare Applications vii
C-Series Touchcomputer for Healthcare Applications viii
European Standards and Classifications
Standards: EN 60601-1-2: 2007
The EMC limits and test methods are referred to the following standards: Emission: Immunity CISPR11:2003+A1:2004 IEC61000-4-2:2008 ED.2.0 +A2: 2006 (Group I, Class A) IEC61000-4-3:2006+A1:2007ED.3.0
CISPR 22: 2005+A1: 2005, Class A IEC 61000-4-4: 2004+A1:2010 ED.2.0 AS/NZS CISPR 22: 2006, Class A IEC 61000-4-5: 2005 ED.2.0 IEC 61000-3-2: 2005 IEC 610004-6: 2008 ED.3.0 +A1: 2008+A2: 2009, Class D IEC 61000-4-8: 2009 ED.2.0 IEC 61000-3-3: 2008 IEC 61000-4-11: 2004 ED.2.0
C-Series Touchcomputer for Healthcare Applications ix
Guidance and manufacturer’s declaration-electromagnetic immunity
for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic emissions
The 19CX/22CX Touchcomputer for Healthcare Applications is intended for use in the electromagnetic environment specified below. The customer or the user of the 19CX/ 22C X Touchcomputer for Healthcare Applications should a ssure that it is used in su ch an environment.
Emissions test
Compliance
Electromagnetic environment-guidelines
RF emissions CISPR 11
Group 1
The 19CX/22CX Touchcomputer for Healthcare App l i c a ti o n s 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 A
Harmonics emissions
IEC 61000-3-2
Class D
Voltage fluctuations/ flicker emissions IEC 61000-3-3
Complies
The 19CX/22CX Touchcomputer for Healthcare Ap pl i c at i o ns is suitable for use in all establishment
s
other than domestic and those directly connected to a low voltage power supply network which supplies buildings used for domestic purposes.
C-Series Touchcomputer for Healthcare Applications x
Guidance and manufacturer’s declaration-electromagnetic immunity
for all EQUIPMENT AND SYSTEMS
Guidance and manufa ctur er’s de claration-ele ctromagnetic immunit
y
The 19CX/22CX Touchcomputer for Healthcare Applications is intended for use in the electromagneti
c
environment specified below. The customer, or the user of the 19CX/22CX Touchcomputer for He alth care App lica tions, should assur e that it is used in such an environment.
Immunity Test Level IEC 60601
Compliance Level Electromagnetic Environment-
Guidelines
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
±
2 kV for power
supply lines
±
1 kV for
input/output
Mains power quality should be that of a typical commerical 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 commerical or hospital
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)
<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)
Mains power quality should be that of a typical commerical or hospital environment. If the user of the 19CX/22CX Touchcomputer for Hea l t h c a r e A p p l i c a t i o n s require s continued operation during power mains interruptions, It is recomme nded th at the 19CX / 2 2C X Touchcomputer 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 commerical or hospital environment.
NOTE UT is the A.C. mains voltage prior to application of the test level.
Guida nce and ma nufa ctur er’s declaration-electr omagnetic i mmunity for all EQUIPMENT AND SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration-electromagnetic immunity
The 19CX/22CX Touchcomputer for Healthcare Applications is intended for use in the electromagnetic environment
specified
below. The user of the 19CX/22CX
Touchcomputer for Healthcare Applications should assure that it is used in such an
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 Vrms
3 Vrms
Portable and mobile RF communications equipment should be used no closer to any part of the
19CX/22CX Touchcomputer for Healthcare Applications and should assure that it is used in such an environment, including cables, than th
e
recommended separation distance calculated from the equation applicabl
e
to the frequency of the transmitter. Recommended separation distance
80MHz to 800 MHz 800 NHz 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
1
, should be less than the compliance level in each frequency range
2
. 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.
C-Series Touchcomputer for Healthcare Applications xi
C-Series Touchcomputer for Healthcare Applications xii
3. 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 19CX/22CX Touchcomputer for Healthcare Applications is used exceeds the applicable RF compliance level above, the 19CX/22CX Touchcomputer 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 19CX/22CX Touchcomputer for Healthcare Applications.
Recommended separation distances between portable
and mobi le R F co mmunications equipmen t and t he 19CX/22CX Touchcomputer for Healthcare Applications for all EQUIPTMENT AND SYSTEMS that are not LIFE-SUPPORTING
Th e 19CX/22CX Touchcomputer for Healthcare Applications is i nte n d ed fo r use in an el ect r omagnetic environment in which radiated RF disturbances are c on tr ol le d. The cu st ome r o r th e us er o f t he 19CX/22CX Touchcomputer for Healthcare Applications can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications (equipment) and the 19CX/22CX Touchcomputer for Healthcare Applications as recommended below according to the maximum output power of t he communications equipment.
Rated Maximum Output Power of Transmitter
(W)
150 kHz to 80 MHz
Separation Distance According to Frequency of Tra nsmitter
80MHz to 800 MHz
800 MHz to 2.5 GHz
0.0 1
0. 1
1 1.
13. 3. 7.4
10
0
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 manufa cturer.
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 aff ecte d by absorption and reflection from structures, objects and people.
0.1 2
0.3 7
1 2
0.1 2
0.3 7
1.
1 2
0.23
0.74
2.3
23
C-Series Touchcomputer for Healthcare Applications User Guide xiii
Table of Contents
Chapter 1: Setup......................................................................................1
Unpacking Your Touchcomputer ..................................................................................................1
Adjusting the Display ....................................................................................................................2
Setting Up the Operating System .................................................................................................2
Calibrating the Touchscreen.........................................................................................................7
Securing the Base.........................................................................................................................9
Chapter 2: Operation.............................................................................10
On-Screen Display (OSD)...........................................................................................................11
L.E.D. Functionality.....................................................................................................................13
Using the Input/Output Panel......................................................................................................14
Chapter 3: Options and Upgrades.......................................................15
Adding Optional Peripherals.......................................................................................................15
Magnetic Stripe Reader (MSR)...................................................................................................16
Customer Display........................................................................................................................18
Fingerprint Reader (FPR) ...........................................................................................................19
Cash Drawer Port Card...............................................................................................................20
Second VGA Port Card...............................................................................................................21
Wireless Card .............................................................................................................................21
Second Hard Disk Drive..............................................................................................................22
Solid State Drive.........................................................................................................................22
Modem Card...............................................................................................................................22
Parallel Port Card........................................................................................................................23
RAID Controller Card..................................................................................................................23
Webcam Kit.................................................................................................................................23
Elo POS Demo Software ............................................................................................................24
Chapter 4: Safety and Maintenance.....................................................25
Safety..........................................................................................................................................25
Care and Handling......................................................................................................................26
Recovering the Operating System..............................................................................................27
Chapter 5: Technical Support...............................................................37
Technical Assistance..................................................................................................................37
C-Series Touchcomputer for Healthcare Applications xiv
Regulatory Information............................................................................38
Warranty ...................................................................................................41
Index ..........................................................................................................43
C-Series Touchcomputer for Healthcare Applications xv
This chapter discusses how to set up and test your touchcomputer. For information on peripheral options, refer to Chapter 3, “Options and Upgrades.”
Unpacking Your Touchcomputer
Check that the following items are present and in good condition:
C H A P T E R
1
SETUP
C-Series Touchcomputer for Healthcare Applications User Guide 1
Adjusting the Display
The display screen can be adjusted from 0 to 70 degrees, as shown below.
CAUTION: To prevent tipping or dropping, be su re to hold the base when adjusting
the display.
Setting Up the Operating System
If configured with an operating system, the initial setup of the operating system takes approximately 5-10 minutes. Additional time may be needed depending on touchcomputer hardware configurations and connected devices.
To set up the Microsoft Windows Operating System for the touchcomputer, turn on the touchcomputer by pressing the power button, and then follow the instructions on the screen.
C-Series Touchcomputer for Healthcare Applications User Guide 2
Injecting the Languages (For Windows 7 OS OS Only)
Windows 7 OS OS Professional only allows the use of one language at one time. But you can use the Elo TouchSystems language injection tool to update your language preference. English is set as the default language, but you can change this language to suit your preferences.
1. After the TE logo shows up, press F8 (frequently) to enter Advanced Boot Options.
2. Select Repair your computer.
3. Click Next OK (Shall not have password)  Click Elo Touch Sy stem Tool.
4. The following UI shall be presented.
5. Click Inject, and the following window will pop out.
C-Series Touchcomputer for Healthcare Applications User Guide 3
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