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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.
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.
•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 vicinity.
•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 harmonized 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.
iv
!
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.
v
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 1 (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 C 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)
o
0
Equivalent to 1013-303 hP.A
(14.7 to 4.4 psia)
For full Product Specifications refer to Appendix C
vi
vii
Table of Contents
Warnings and Cautions ................................................. iv
Caution-Life Support ...................................................... v
Classification .............................................................. vi
Solutions to Common Problems ................................. 17
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 no 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