K5902133 (451920612483)-02 MDSC-8255
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• Sufficient 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.
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
• 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
• 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 enclosure has to be checked upon collision damage, refer to qualified service personnel
This apparatus conforms to:
Medical Equipment:
• IEC 60601-1: 2012 Edition 3.1 (Medical electrical equipment – Part 1: General requirements for basic
safety and essential performance)
• EN 60601-1: 2006 +A1:2013 (Medical electrical equipment”. Part 1: General requirements basic safety and
essential performance)
• ANSI/AAMI ES 60601-1: 2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A2:2010/(R)2012 - Med. El.
Equip., Part 1: general req. for basic safety and essential performance.
• CAN/CSA-C22.2 No. 60601-1: 14 Medical Electrical Equipment - Part 1: General Requirements for Basic
Safety and Essential Performance (Harmonized with Ed. 3.1)
EMC:
• IEC 60601-1-2 (4th Ed)
• EN 55011 / CISPR11 (MDSC-8255: Class B)
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"
Important information
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