Barco E192HSA, User Manual

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6. Important information
Installation
• Place the equipment on a fl at, solid and stable surface that can support the weight of at least 3 units.
If you use an unstable cart or stand, the equipment may fall, causing serious injury to a child or adult,
and serious damage to the equipment.
• Do not allow to climb or rest on the equipment.
• When adjusting the angle of the equipment, move it slowly so as to prevent the equipment from moving
from or slipping off its stand or arm.
• 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.
• Provide full attention to safety during installation, periodic maintenance and examination of this equip-
ment.
• Suf fi cient expertise is required for installing this equipment, especially to determine the strength of the
wall, arm or ceiling suspension for withstanding the display’s weight. Be sure to entrust the attachment
of this equipment to the wall to a duly skilled technician and pay adequate attention to safety during
the installation and usage.
• The manufacturer is not liable for any damage or injury caused by mishandling or improper installation.
General warnings
• 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 monitor fails.
Technical data
• The monitor is intended for indoor use
• The monitor has been designed to be used in landscape position with a tilt of -10° backward and +10°
forward.
• Class I Equipment, according to the type of protection against electric shock
• The monitor is not intended to be sterilized
• The monitor has no applied parts. The front side of the monitor and the plastic enclosure have been
treated as applied parts however, because they may accidentally be touched by the patient for a time
<1 minute.
• The compliance of this display with Medical Safety and EMC requirements has been evaluated using
the external (optional) medical power supply Skynet model ’BAR-A159’. If a different power supply will
be used, further investigation for Safety and EMC requirements have to be performed at system level.
• The enclosure has to be checked upon collision damage, refer to quali fi ed service personnel.
This apparatus conforms to:
• MDD 93/42/EEC (Class1), Amended by 2007/47/EC
• EN 60601-1 3rd Edition (2006) - Medical Electrical Equipment / General Requirements for basic Safety
and essential performance
• IEC 60601-1 3rd Edition (2005) - Medical Electrical Equipment / General Requirements for basic Safety
and essential performance
• ANSI/AAMI ES60601-1 3rd Edition (2005) - Medical Electrical Equipment / General Requirements for
basic Safety
• CAN/CSA-C22.2 No. 60601-1 (2008) - Medical Electrical Equipment - Part 1: General Requirements
for basic Safety and Essential Performance
• CE c-UL-us, DEMKO, PSE (available on PSU), CCC
• EMC Medical EMC Standards: IEC/EN 60601-1-2 (2007), EN55011/CISPR 11 (Class B), FCC CFR47
part 15 & 18
• RoHS-2, REACH, WEEE compliant
K5902113 ( 451920611383 ) E192HSA 27/11/2017 37