Planar Dome C2 Reference Manual page 4

QUICK LINKS
Contents
Index
Regulatory Compliance
Product Information
Warranty
GETTING STARTED
About the Display
Package Contents
Identify Components
Position Display
Desk Stand Features
INSTALLING THE DISPLAY
Set DIP Switch
Install Display Controller
Connect Video and Power
Install Display Driver
Configure Display Settings
Configure Windowing
DPMS Screen Saver
Console Modification
Dome CXtra Software
APPENDIXES
Troubleshooting
Specifications
Video Modes
Connector Ports
LED Status Lights
USB Connection
Regulatory Compliance
Dome CX displays have been tested and found to comply with IEC/EN 60601-1 and
IEC/EN 60601-1-2 standards, and are certified to meet medical standard C22.2 No. 601.1-M1990
(C US Mark).
The medical display, in addition to meeting medical requirements, has been tested and found to
comply with the limits for Federal Communications Commission (FCC) Class B computing devices in
a typically configured system since many medical offices are located in residential areas. It is the
system integrator'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
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.
Dome CX Display System for Solaris
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