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
DateDescription
July 2000Document number OM700-02 (020-0151-00 Rev. C)
Contents
Planar D6015TM Series Medical Monitor........................................................1
Figure 12: Desk Stand Option....................................................................................22
iiOperations Manual (OM700-02)
Planar D6015TM Series Medical Monitor
The Planar D6015TM Series Medical Monitor is a 15-inch XGA monitor
designed to be versatile, ergonomic, and easy to use. It is capable of displaying
most video standards from 640x480 (VGA) to 1024x768 (XGA). The digital
controls located on the front panel allow you to easily adjust the monitor’s
display parameters using the On-Screen Display (OSD) menus.
Using either a VESA/GCX Instrument Mounting System or compatible
mounting plate or an optional desk stand, the monitor’s small footprint allows
you more room in your workspace for other peripherals. The two stereo speakers
let you further expand your computer’s multimedia capabilities by connecting
your system’s audio-out port to the monitor’s audio-in port.
The architecture of the Planar D6015TM Series Medical Monitor incorporates
an active matrix LCD (AMLCD) panel that produces a clear display with low
radiation emission, greatly reducing the radiation-related health concerns
associated with CRT monitors.
Functional Description
The Planar D6015TM Series Medical Monitor consists of a low-profile molded
plastic monitor head, video and audio cables, and a power supply. Options
include a Surface Acoustic Wave or Resistive touchscreen with interface cable.
The display shows 262,144 colors with a pixel matrix of 1024 columns by 768
rows.
The monitor is compatible with standard analog computer video signals. It is
connected to the host computer through a standard 15-pin VGA connector on the
bottom of the monitor.
The monitor automatically adjusts to applied video and synchronization signals
to provide a stable, centered display. Additionally, user controls for brightness
and tuning are located on the front of the monitor.
The monitor is certified by TÜV Rheinland according to IEC/EN60601-1:1990
+A1 + A2 for sale to the medical market. The monitor is certified by CSA
International to medical standards C22.2 No. 601.1-M1990 (C US Mark)
(equivalent to UL2601). The monitor is also CE marked for sale into the
European Community for integration or use with medical products.
Operations Manual (OM700-02)1
Product Features
• Display Type: Color Active Matrix LCD
• Control Buttons:
− Function select up and Function select down ( and )
− Adjustment increase and Adjustment decrease ( and )
− Power on/off ( )
• Adjust speaker volume directly with the Adjustment increase/decrease
buttons.
• Indicators:
− On-Screen Display “OSD” function
− Power LED indicator is lit when the monitor is on and blinking when the monitor
• Display Formats:
− VGA, SVGA, and XGA
− VESA DDC1 and DDC2B Plug and Play Functions
− NEC PC98
− APPLE MAC
− 1024x5l2 (special)
is in power-save/standby mode
Cleaning Instructions
The D6015TM Series Monitors will continue to operate normally while being
cleaned in a fashion normal for a hospital environment. This includes cleaning
with a damp (wrung out), mild soapy cloth. Protection from various chemicals
used for cleaning, and protection from liquids consistent with these cleaning
procedures is provided in accordance with IPX1 rating per IEC/EN60529.
The D6015TM Series Monitors will withstand non-abrasive cloths and cleaning
solutions used in hospitals for like equipment. This is typically warm water and
mild detergent for all surfaces or 70% IPA for the touchscreen surface. Possible
chemicals include:
• 70% isopropyl alcohol
• 1.6% aqueous ammonia
• Cidex (2.4% glutaraldehyde solution)
• Sodium Hypochlorite (bleach) 10%
• “Green soap” USP
• 0.5% Chlorhexidine in 70% isopropyl alcohol
• Ovation®
• Formula 409®
• Fantastic®
• WexCide®
To clean the screen, do not spray liquid cleaners directly onto the unit. Stand away
from the monitor and spray cleaning solution onto a cloth. Without applying
excessive pressure, clean the screen with the slightly dampened rag.
2Operations Manual (OM700-02)
Safety Instructions
• Do not place your 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 in an area 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. Refer all
servicing to qualified personnel to maintain warranty.
• When using the monitor with the desk stand option, it must be placed on a flat
surface that is horizontal to ±5°.
• 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 this
range could result in permanent damage. Please store in the original shipping carton.
• If any cord or cable is frayed or damaged, immediately replace it with a another of
the same type and rating as supplied by Planar. See “Ordering Information” for part
numbers. Safety and regulatory listings and certifications do not apply if other
cables are used.
• If the monitor has been exposed to liquid, or it has been dropped, or the case has
been damaged, it may pose a shock or fire hazard; immediately unplug it and
contact customer service for assistance.
• Use only Planar Power Adapter (model PPA4512UM) which has been tested and
approved for use with this monitor product. See “Ordering Information” for part
numbers.
Caution: AC Adapter must be plugged into a GROUNDED power outlet.
• When cleaning the power adapter, use a cloth dampened with liquid cleaners on the
outside of the enclosure only. Do not immerse product in liquid or a safety hazard
could arise during use.
• Do not use the power adapter in the presence of flammable anesthetics.
Disposal Information
This monitor contains cold cathode fluorescent lamps which contain a maximum of
12 mg (3 mg per lamp) of mercury. Please follow local ordinances or regulations for
its disposal.
Operations Manual (OM700-02)3
Symbol Explanations
Following are explanations of the symbols found on the monitor or power supply.
Indicates proof of conformity to applicable European Economic
Community Council directives and to harmonized standards
published in the official journal of the European Communities.
Tested and certified by CSA to C22.2 N0. 601.1-M1990. If this
mark appears with the indicators “C” and “US” the product is
certified for both the U.S. and Canadian markets, to the applicable
U.S. and Canadian standards.
Tested to comply with FCC Class B standards.
Indicates that the monitor has been designed to meet low radiation
standards.
Consult accompanying documents.
Tested and certified by TÜV Rheinland in accordance with
EN60601-1.
Indicates protective earth ground.
For indoor use only.
Identifies the socket for headphones.
Regulatory Compliance
This monitor has been tested to comply with IEC/EN 60601-1 and IEC/EN 60601-1-2
by TÜV Rheinland and is certified by CSA International to medical standards C22.2
No. 601.1-M1990 (C US Mark).
Because many medical offices are located in residential areas, this monitor, in addition
to the medical requirements, has also been tested and found to comply with the limits
for 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 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 council directive 93/42/EEC –
commonly referred to as the Medical Device Directive (MDD). The following is a summary of our
qualification of these displays as it relates to compliance with the MDD.
The European Medical Device Directive requires that the intended use of a device be defined. The
intended use of these displays is “to display alpha numeric, 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/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 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
4 Operations Manual (OM700-02)
classified according to Rule 12 as an MDD Class I device – component or accessory. The MDD
sets out that manufacturers of Class I medical devices or accessories shall satisfy the
requirements in regards to design and manufacturing controls, i.e. the applicable assessment
route to be used for CE-marking under the MDD and shall carry the CE-mark according to Annex
XII of the directive, with no notified body annotation.
The applicable safety standards for a MDD Class I display are IEC/EN 60601-1: 1990 along with
Amendments 1 & 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 do not represent a functional medical device. Hence, Planar
has configured a minimal operating system that exercised the display. The resulting data is made
available to interested parties.
This 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 EC declaration of conformity.
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 EEA, has a European Representative, Planar Systems, Inc. – Espoo, Finland.
It is the opinion of Planar Systems, Inc. that registration of putting into commerce is the
responsibility of the medical device/system manufacturer and Planar supports this requirement by
providing an EC declaration of conformity. If Planar supplies a display to an end user, rather than
a device manufacturer, it is the end users responsibility to assure continued compliance of the
system in which the display is being integrated with the MDD.
For Vigilance reporting as required under Article 10 of the MDD, Planar Systems, Inc. will
provide any information requested by a competent authority to support any reported incident
investigation by such an authority.
EU Declaration of Conformity for Medical Applications
A Declaration of Conformity has been filed for this product. A sample of this
document may be found in the addendum which accompanied this manual. For a copy
of the Declaration of Conformity document, please contact Planar Systems, Inc. and
request document number 001-0014-00 “Declaration of Conformity”.
Operations Manual (OM700-02)5
Installation
Before you unpack your monitor, prepare a suitable workspace. You need a
stable and level surface near a grounded wall outlet in an area which is relatively
free of glare from sunlight or other sources of bright light. The monitor is cooled
by natural convection (it has no fan). For optimum performance, do not block the
cooling vents.
While unpacking the monitor, inspect it and other package contents for shipping
damage that could cause a fire or shock hazard. Immediately report any shipping
damage to the carrier or transportation company and contact customer service for
assistance. Keep all packing material in case you need to ship or store the
monitor in the future or in case of return.
After you unpack the monitor, make sure the following items are included (refer
to “Ordering Information” for part numbers):
• Monitor with 1.5 meter (5 ft.) monitor-to-computer video cable
• 1.5m (5 ft.) stereo audio cable
• AC adapter with cable. (CAUTION: AC Adapter must be plugged into a
GROUNDED power outlet.) Output power: 12Vdc to a 4 pin male locking
mini-din connector.
• Power cord (medical grade) which connects from AC mains to AC adapter.
• Touchscreen cable if monitor has touchscreen option.
• This operations manual
Note: Your system provider may offer alternative cords or cables
depending on the installation requirements and local geography issues.
6Operations Manual (OM700-02)
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