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6. Important information
58
MEDICAL – GENERAL MEDICAL EQUIPMENT
AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH ANSI/AAMI AS60601-1:2005/(R)2012, CSA
CAN/CSA-C222.2 NO. 60601-1:14
Indicates the device is approved according to the UL Demko regulations
Indicates the device is approved according to the CCC regulations
Indicates the device is approved according to the VCCI regulations
Indicates the device is approved according to the KC regulations
Indicates the device is approved according to the BSMI regulations
Indicates the device is approved according to the PSE regulations
Indicates the device is approved according to the RCM regulations
Caution: Federal law (United Stated of America) restricts this device to sale by
or on the order of a licensed healthcare practitioner.
Indicates the device is approved according to the BIS regulations
Indicates the USB connectors on the device
Indicates the DisplayPort connectors on the device
Indicates the legal manufacturer
Indicates the manufacturing date
K5902135 (451920612561) MDSC-2326 28/02/2017
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