Environmental Information - Barco Eonis MDRC-2222 WP User Manual

22-inch clinical display
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Important information
Installation
Place the device on a flat, solid and stable surface that can support the weight of at least 3 devices. If you
use an unstable cart or stand, the device may fall, causing serious injury to a child or adult, and serious
damage to the device.
The display has been designed to be used in landscape and portrait position with a tilt of -5° to 22°.
When the equipment is attached to an arm, do not use the equipment as a handle or grip in order to move
the equipment. Please refer to the instruction manual of the arm for instructions on how to move the arm
with the equipment.
All devices and complete setup must be tested and validated before taking into operation.
At end user application level it is necessary to foresee a backup unit in case the video falls away.
Malfunctions
Disconnect the equipment's power cord from the AC inlet and refer servicing to qualified service technicians
under the following conditions:
If the power cord or plug is damaged or frayed.
If liquid has been spilled into the equipment.
If the equipment has been exposed to rain or water.
If the equipment does not operate normally when the operating instructions are followed. Adjust only those
controls that are covered by the operating instructions since improper adjustment of other controls may
result in damage and will often require extensive work by a qualified technician to restore the product to
normal operation.
If the equipment has been dropped or the cabinet has been damaged.
If the product exhibits a distinct change in performance, indicating a need for service.
General warnings
The device has no means to be incorporated in an IT-network in the clinical environment.
The enclosure has to be checked upon collision damage, refer to qualified service personnel.
The protective screen (if present) is made of tested high-resistance glass. Nonetheless there is the
possibility that it may crack if subject to strong impacts. Evaluate and prevent the risk of possible
breakages of the protective screen by correctly handling and positioning the monitor in the operating room.
The monitor is intended for indoor use
The monitor is not intended to be sterilized
The monitor has not applied parts, but the front side of the LCD panel and the plastic enclosure have been
treated as applied part because considered accidentally touchable by the patient for a time <1 minute.
National Scandinavian Deviations for CL. 1.7.2
Finland: "Laite on liitettävä suojamaadoituskoskettimilla varustettuun pistorasiaan"
Norway: "Apparatet må tilkoples jordet stikkontakt"
Sweden: "Apparaten skall anslutas till jordat uttag"

5.2 Environmental information

Disposal Information
Waste Electrical and Electronic Equipment
This symbol on the product indicates that, under the European Directive 2012/19/EU governing waste
from electrical and electronic equipment, this product must not be disposed of with other municipal waste.
Please dispose of your waste equipment by handing it over to a designated collection point for the recycling of
waste electrical and electronic equipment. To prevent possible harm to the environment or human health from
uncontrolled waste disposal, please separate these items from other types of waste and recycle them
responsibly to promote the sustainable reuse of material resources.
30
K5902146 (451920612625) /04
Eonis

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