About the Display
Display Installation
Display Controls
Troubleshooting
Ordering Parts
Warranty
Americas Sales
Planar Systems, Inc.
1195 NW Compton Drive
Beaverton, OR 97006-1992 USA
(503) 748-1100 phone
(503) 748-1493 fax
Medical Sales
Planar Systems, Inc.
400 Fifth Avenue
Waltham, MA 02451-8738 USA
(781) 895-1155 phone
(781) 895-1133 fax
Europe & Asia-Pacific Sales
Planar Systems, Inc.
Olarinluoma 9, P. O. Box 46
FIN-02201 Espoo, Finland
+ 358 9 420 01 phone
+ 358 9 420 0200 fax
Internet address for sales information: medicalsales@planar.com
Internet address for technical support: medicalsupport@planar.com
World Wide Web site: www.planar.com
guarantee is given to the correctness of the contents. This document is subject to
change without notice. Planar provides this information as reference only. Reference
to other vendors’ product does not imply any recommendation or endorsement.
This document contains proprietary information protected by copyright. No
part of this manual may be reproduced by any mechanical, electronic, or other
means, in any form, without prior written permission of the manufacturer.
Planar is a registered trademark and VitalScreen is a trademark of Planar Systems, Inc.
DOCUMENT HISTORY
DateDescription
September 2002020-0247-00 Rev. A
August 2003020-0247-00 Rev. B
October 2003020-0247-01 Rev. A
This display has been tested and certified to international medical safety
standards IEC/EN 60601-1 and IEC/EN 60601-1-2, and is certified to meet
C22.2 No. 601.1-M1990 (C US Mark).
Because many medical offices are located in residential areas, the medical display,
in addition to meeting medical requirements, has also been tested and found to
comply with the limits for Federal Communications Commission (FCC) Class B
computing devices in a typically configured system. It is the system integrator or
configurer’s responsibility to test and ensure that the entire system complies with
applicable electromagnetic compatibility (EMC) laws.
Planar Systems, Inc. has made great efforts to support the medical device industry,
in particular, medical device manufacturers and medical device system integrators.
We offer state-of-the-art color displays that are compliant with worldwide accepted
medical device safety standards, and for the European market, CE-marked displays
based on compliance with counsel directive 93/42/EEC commonly referred to as the
Medical Device Directive (MDD). The following summarizes our qualification of these
displays as it relates to compliance with the MDD.
The European Medical Device Directive requires that the intended use of the device
be defined. The intended use of these displays is “to display alphanumeric, graphic,
and image data as inputted from any type of medical device.” These displays do not
provide a measurement function in any way, and it is the device and systems
manufacturer’s responsibility to verify its function in the integrated device or system.
The display was classified as required by the MDD according to Annex IX of the
directive and the medical device (MEDDEV) guidance available at the time of
classification. Because the display uses electrical energy and has no direct patient
connections and—by itself—no medical utility, the display is classified according to
Rule 12 as an MDD Class I device-component or accessory. The MDD states that
manufacturers of Class I medical devices or accessories shall satisfy the requirements
in regard to design and manufacturing controls, that is, the applicable assessment
route to be used for CE-marking under the MDD, and it shall carry the CE mark
according to Annex XII of the directive, with no notified body annotation.
The applicable safety standards for an MDD Class I display are IEC/EN 60601-1:1997
along with Amendments 1 and 2. To help the medical device designer evaluate the
suitability of these displays, Planar has also conducted EMC testing to IEC 60601-1-2
as it can be applied. The display with its power supply alone does not represent a
functional medical device. Hence, Planar configured a minimal operating system to
exercise the display. The resulting data are made available to interested parties.
The data are informative data, not certification data. Certification data must be
obtained by the device or system integrator according to Article 12 of the MDD titled
“Particular procedure for systems and procedure packs.” Paragraph 2 clearly outlines
the device or system integrator’s responsibility in this matter.
In summary, Planar Systems, Inc. is CE-marking these displays under the Medical
Device Directive, which establishes compliance to the basic medical safety standards.
However, EMC compliance can only be accomplished in the configured medical
device or system and is the responsibility of the device or system manufacturer.
Planar has the necessary documentation such as IEC 60601-1 notified body and
other third-party test reports and certifications, a risk/hazard analysis, an essential
requirements checklist, and the Planar International Electrotechnical Commission
(IEC) declaration of conformity.
v
Planar Systems, Inc., located in Beaverton, Oregon, USA, is the manufacturer of these
displays in the meaning of the directive. As required by the MDD in Article 14, Planar
Systems, Inc., not residing in the European Economic Area (EEA), has a European
representative, Planar Systems, Inc.—Espoo, Finland.
In the opinion of Planar Systems, Inc. registration required to put this device into
commerce is the responsibility of the medical device/system manufacturer, and
Planar supports this requirement by providing a European commission (EC)
declaration of conformity. If Planar supplies a display to an end user, rather than
a device manufacturer, it is the end user’s responsibility to ensure continued
compliance with the MDD of the system in which the display is integrated.
For vigilance reporting as required under Article 10 of the MDD, Planar Systems, Inc.
will provide any information requested by competent authority to support any
reported incident investigation by such an authority.
European Union Declaration of Conformity for Medical Applications
A Declaration of Conformity has been filed for this product. For additional copies of
the Declaration of Conformity document, contact Planar Systems, Inc. and request
document number 001-0014-07 “Declaration of Conformity.”
About
This Manual
This manual contains information on the setup, use, and proper
maintenance of VitalScreen
S 15" display models VSS15X (non-touch)
™
and VSS15X-TR (resistive touch). Keep this manual for future reference.
The section on product information provides safety and cleaning
instructions. It also explains the symbols used on the products.
Chapter 1provides an overview of the VitalScreen S display. It lists the
contents of the display package and identifies the components of the
display. Chapter 2 explains how to install the display correctly and use
optional components. Chapter 3explains the menus and function
controls built into the display.
Appendix A shows technical information. Appendix B gives supported
timing. Appendix C offers troubleshooting solutions.
Description of warranty and ordering information are provided at
the back of this manual.
vi
Product Information
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Safety
instructions
Store the display in its original shipping carton when it is not in
operation for extended periods of time. Also use the original packing
materials and carton when shipping the display.
Do not place the display near a window. Exposing the display to rain,
water, moisture, or direct sunlight can damage it.
Do not place anything on top of the video cable. Make sure
the cable is placed where it will not be stepped on.
Do not apply excessive pressure to the screen. Excessive
pressure may cause permanent damage to the display.
Refer all servicing to qualified personnel to maintain your
warranty. The display and power adapter units contain no
user-serviceable parts.
Do not cover or obstruct the venting holes on the back of
the display.
Store the display in an environment with a temperature range
from -20 to 65 degrees Celsius. Storing your display outside that
temperature range could result in permanent damage.
Do not expose the display to liquid or drop it. If the case has been
damaged, the unit may pose a shock or fire hazard. Unplug the unit
immediately and call customer service for assistance.
Replace any cord or cable that is frayed or damaged with another
of the same type and rating, as supplied by Planar. The safety and
regulatory listings and certifications are based on the cable supplied
by Planar.
Use only the power adapter that has been tested and approved for
use with this display product. The power adapter must be plugged
into a grounded power outlet.
Do not immerse the power adapter in liquid, or a safety hazard could
arise during use.
Do not use the power adapter near inflammable anesthetics.
1
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vii
Cleaning
instructions
Use only the products listed below for cleaning the display. The
products differ for cleaning the screen and cleaning the plastic
enclosure. Be sure you use only the specific products approved for
either the screen or the enclosure.
Always apply the product to a clean nonabrasive cloth and then wipe
the screen or plastic enclosure. Cleaners applied directly to the display
could leak inside a non-sealed unit and cause damage. Be careful not to
splash solvents on the screen or enclosure.
Recommended cleaning solution for screen
Use 70 percent isopropyl alcohol. This is the only cleaning solution
approved for use on the non-touch screen (model VSS15X) and the
touch screen (model VSS15X-TR).
Do NOT use water or solvents (such as ketone, acetone) and aromatics
(such as xylene, toluene).
To clean the screen
Switch the power off.
Dampen a clean nonabrasive cloth with 70 percent
isopropyl alcohol.
Wipe the screen gently with the dampened cloth.
Dry the screen with a clean nonabrasive cloth to remove
any residue.
Recommended cleaning solutions for plastic enclosure
You may also use 70 percent isopropyl alcohol to clean the plastic
enclosure. Otherwise, use only these approved products to clean
the enclosure.
Cidex®
Clorox Clean-Up®
“Green soap” United States Pharmacopoeia (USP)
Formula 409®
Sani-Cloth® Plus
Virustat TBQ™
Do NOT use these products on the screen.
viii
Symbol
explanations
This table explains the symbols appearing on the display or
power adapter.
SymbolDescription
Proof of conformity to applicable European
Economic Community Council directives and
two harmonized standards published in the
official journal of the European Communities.
The product has been tested and certified by
CSA to C22.2 No. 601.1-M90. If this mark appears
with the indicators "C" and "US," the product
is certified for the Canadian and U.S. markets,
meeting the applicable Canadian and
U.S. standards.
The product has been tested to comply with
FCC Class B standards.
The product has been tested and certified by
TÜV Rheinland in accordance with EN6061-1.
More information available in
accompanying documents.
Protective earth ground.
Indoor use only.
Socket for headphones.
About the VitalScreen S
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The architecture of the VitalScreen
panel that produces a clear display with low radiation emission. This
technology greatly reduces the radiation-related health concerns
associated with CRT monitors.
More significant, the VitalScreen S display is medically certified under
UL 2601 and IEC 60601. These qualifications make the display safer for
the patient and protect the hospital from liability.
Your new VitalScreen S display is versatile, ergonomic, and userfriendly. It supports Plug and Play and displays most standards from
640 x 480 VGA to 1024 x 768 XGA. The digital controls located on the
front panel allow you to easily adjust the display parameters using
onscreen menus. When incorporated into a complete workstation,
the display can be wall-mounted for added convenience.
Selecting a Workspace
Before you unpack the VitalScreen S display, select a suitable
workspace for the display and computer. You need a stable, level, and
clean surface near a wall outlet.
Even though this display uses little power, place it in a location that
allows sufficient airflow to ensure proper ventilation.
Avoid setting up the display near a window where sunlight often
comes in. You will have difficulty seeing the screen with glare reflecting
off the display.
S display incorporates an AMLCD
™
Unpacking the Display
Make sure you receive the following items. If any item is missing or
damaged, see your dealer immediately.
LCD screen
Desk stand or VESA mounting plate
Video cable
Stereo audio cable
Touchscreen cable (VSS15X-TR only)
AC power adapter with 1.5-meter (5-foot) cable
Medical-grade power cord (US or European)
CD with touchscreen driver and PDF of this manual
EU Declaration of Conformity
2 Model VSS15X / VSS15X-TR
Identifying the Components
The VitalScreen S display provides easy access to all controls and
peripheral ports. The following illustrations of the front and back
panels identify the display controls and ports.
Front panel
1
2
3
4
5
6
7
1LCD screenA 15-inch diagonal AMLCD. The screen
supports a maximum resolution of
1024 x 768 (XGA).
2Function UP and
DOWN buttons
3Adjust PLUS and
MINUS buttons
4Power ON/OFFPower switch.
5LED power indicator A light-emitting diode (LED) indicator that
Vertical arrows to navigate the onscreen
display menu horizontally. UP selects the
functions to the left. DOWN selects the
functions to the right.
Controls to change the value of
the selected function.
stays lit when the power is on and the
display is receiving a proper video signal.
The LED blinks slowly when the display is
in power-saving mode.
6Stereo speakersTwo transmission channels for sound.
7Desk standFlat-surface support for the display. The
stand allows you to pivot the screen to
various viewing angles.
Back panel
About the VitalScreen S 3
412
3
1Audio Line InJack for the audio cable. (You can also
connect the CD-ROM Line Out to this jack.)
2Power input port
(locking mini
DIN connector)
3Video connector port Port for a 2-meter cable with two 15-pin
4Touchscreen portPort for the RS-232 cable; used to operate
Port for the power connector.
D-Sub VGA connectors; used to join the
display to the VGA card in your computer.
the optional touch screen. This cable
is provided with the Optional Touch
Screen package.
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