6. Important informationInstallation• Place the equipment on a flat, 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 movingfrom 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 tomove the equipment. Please refer to the instruction manual of the arm for instructions on how to movethe arm with the equipment.• Provide full attention to safety during installation, periodic maintenance and examination of this equip-ment.• Sufficient expertise is required for installing this equipment, especially to determine the strength of thewall, arm or ceiling suspension for withstanding the display’s weight. Be sure to entrust the attachmentof this equipment to the wall to a duly skilled technician and pay adequate attention to safety duringthe 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 beentreated 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 usingthe external (optional) medical power supply model ’XP Power AHM250PS24T’. If a different powersupply will be used, further investigation for Safety and EMC requirements have to be performed atsystem level.• The enclosure has to be checked upon collision damage, refer to qualified service personnelThis apparatus conforms to:Medical Equipment:• IEC 60601-1: 2012 Edition 3.1 (Medical electrical equipment – Part 1: General requirements for basicsafety and essential performance)• EN 60601-1: 2006 +A1:2013 (Medical electrical equipment”. Part 1: General requirements basicsafety 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 forBasic Safety and Essential Performance (Harmonized with Ed. 3.1)EMC:• IEC / EN 60601-1-2: 2007• EN 55011 / CISPR11 (MDSC-8231: Class B)K5902130 (451920612471) MDSC-8231 04/11/2016 39