This document is subject to change without notice. Planar provides this information as reference
only. Reference to other vendors’ products does not imply any recommendation or endorsement.
Revision Control
Date Description
May 2001 Document number OM705-00 (020-0158-00 Rev. A)
Contents
Planar VS15XAD VitalScreen Medical Grade Monitor Family.....................1
Figure 10. Color Menu ......................................................................................14
Figure 11. Digital Basic Menu ..........................................................................15
Figure 12. Digital Miscellaneous Menu ...........................................................15
ii
Operations Manual (OM705-00)
Planar VS15XAD VitalScreen Medical Grade
Monitor Family
The Planar VS15XAD VitalScreen Medical Grade Monitor family is a set of
high-resolution color monitors designed to be versatile and easy to use. These
monitors can accept either analog or digital video input and display most video
standards from 640 x 480 (Video Graphics Array, or VGA, standard) to
1024 x 768 (Extended Graphics Array, or XGA, standard). The controls located
on the front panel allow you to easily adjust the monitor’s display parameters
using on-screen display (OSD) menus.
The monitor’s video input is a single-link, transition minimized differential
signaling (TMDS) digital visual interface (DVI) and is compliant with the
Digital Display Working Group (DDWG) DVI standard. This interface produces
the sharpest display image possible with little need for adjustment. Setup is
simple: just plug in the monitor and use.
The monitor uses a mounting plate that conforms to the Video Electronics
Standards Association (VESA) mounting standard
1
. That configuration allows
the monitor to be mounted in a variety of ways, such as on a wall bracket or
swing arm. An alternate configuration with a desk stand is also available for easy
use on flat work surfaces.
The architecture of the Planar VS15XAD VitalScreen Medical Grade Monitor
incorporates an active matrix liquid-crystal display (AMLCD) panel that
produces a clear display with low radiation emission, greatly reducing the
radiation-related health concerns associated with cathode-ray tube monitors.
1
The VESA Flat Panel Monitor Physical Mounting Interface (FPMPMI) Standard defines
physical mounting interfaces for flat panel monitors, corresponding standards for flat
panel monitor mounting devices and associated cable, cable connectors and power supply
location guidelines. For more information, see http://www.vesa.org/
Operations Manual (OM705-00)
.
1
Cleaning Instructions
The VS15XAD VitalScreen Medical Grade Monitor will continue to operate
normally while being cleaned in a fashion normal for a hospital environment.
That includes cleaning with a damp (wrung out), mild soapy cloth. Drip
protection is provided in accordance with IPX1 rating defined in the
IEC/EN60529 standard.
The VS15XAD VitalScreen Medical Grade Monitor family withstands
nonabrasive cloths and cleaning solutions used in hospitals for like equipment.
That would typically include warm water and mild detergent for all surfaces or
70 percent isopropyl alcohol for the touch-screen surface. Possible cleaning
solutions include these:
70 percent isopropyl alcohol
•
1.6 percent aqueous ammonia
•
Cidex® (2.4 percent glutaraldehyde solution)
•
Sodium hypochlorite (bleach) 10 percent
•
“Green soap” United States Pharmacopoeia
•
0.5 percent Chlorhexidine in 70 percent isopropyl alcohol
•
Ovation®
•
Formula 409®
•
Fantastic®
•
•
WexCide
To clean the screen, do not spray liquid cleaners directly onto it. Stand away from the
monitor and spray the cleaning solution onto a nonabrasive cloth. Without applying
excessive pressure, clean the screen with the slightly dampened cloth.
®
863
Safety Instructions
•
Do not place the monitor near a window. Exposing the monitor to rain, water,
moisture or constant direct sunlight can severely damage it.
•
Do not place anything on top of the monitor-to-computer signal cord. Make sure the
cord 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.
•
The monitor and power supply units have no user-serviceable parts inside, except
for the backlight lamp assemblies. Refer all servicing to qualified personnel to
maintain your warranty.
•
Do not cover or obstruct the venting holes on the back of the monitor.
Store the monitor within -20° to +65° Celsius. Storing your monitor outside
•
that temperature range could result in permanent damage. Please store the
monitor in its original shipping carton.
•
If any cord or cable is frayed or damaged, immediately replace it with another of the
same type and rating as supplied by Planar. See “Ordering Information” on page 22
for part numbers. The safety and regulatory listings and certifications are based on
the cable supplied by Planar.
•
If the monitor has been exposed to liquid, it has been dropped, or if its case has been
damaged, it may pose a shock or fire hazard; immediately unplug it and contact
customer service for assistance.
2
Operations Manual (OM705-00)
Use only the power adapter that has been tested and approved for use with
•
this monitor product. See “Ordering Information” on
numbers.
Caution: The power adapter must be plugged into a GROUNDED
power outlet.
To clean the power adapter, use a cloth dampened with liquid cleaner on the
•
outside of the enclosure and cable only. Do not immerse the product in liquid,
or a safety hazard could arise during use.
page
22 for part
Do not use the power adapter near flammable anesthetics.
•
Disposal Information
This monitor contains cold cathode fluorescent lamps, which contain a maximum
of 12 milligram (3 milligram per lamp) of mercury. Please follow local
ordinances or regulations for its disposal.
Regulatory Compliance
This monitor has been tested and found to comply with IEC/EN 60601-1 and
IEC/EN 60601-1-2 standards by TÜV Rheinland and is certified by CSA
International to meet medical standard C22.2 No. 601.1-M1990 (C US Mark).
Because many medical offices are located in residential areas, the medical
monitor, in addition to meeting medical requirements, has also been tested and
found to comply with the limits for Federal Communications CommissionFCC)
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 manufacturers 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, i.e., 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.
Operations Manual (OM705-00)
3
The applicable safety standards for an MDD Class I display are IEC/EN 606011: 1990 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 is made
available to interested parties.
The data is 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 Planar’s
International Electrotechnical Commission (IEC) declaration of conformity.
Planar Systems, Inc. located in Beaverton, OR, 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 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 Economic Area (
EEA) has a
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, please contact Planar
Systems, Inc. and request document number 001-0014-03 “Declaration of
Conformity.”
4
Operations Manual (OM705-00)
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