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Planar VS17SXAD User Manual

Page 5

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VS17 Display

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QUICK LINKS

Contents

FCC Compliance Statement

Index

Ordering Parts

Product Information

Regulatory Compliance

Warranty

GETTING STARTED

About the Display

Unpack Display

Identify Components

Adjust Orientation/Angle

INSTALLING THE DISPLAY

Connect Power

Connect Video

Connect Audio

Connect Touch Screen

Power Management System

USING THE CONTROLS

Overview

Hot Key Functions

OSD Menu

Function Menus

OSD Lockout

APPENDIXES

Technical Information

Supported Timing

Troubleshooting

This 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 the Planar International Electrotechnical Commission (IEC)
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 European Economic Area (EEA), has a European representative, Planar Systems, Inc.—
Olarinluoma 9, P.O. Box 46, FIN-02201Espoo, Finland (phone + 358 9 420 01; fax +358 9 420 0200).

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.

This manual is related to the following products: