Barco Eonis MDRC-2222 WP User Manual page 37

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-C22.2
E346057
NO. 60601-1:14
Indicates the device is approved according to the UL regulations for Canada and US.
E346057
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.
Indicates the device is approved according to the EAC 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.
IS 13252 (Part 1)
IEC 60950-1
R-xxxxxxxx
www.bis.gov.in
Indicates the device is approved according to the INMETRO regulations.
Indicates the USB connectors on the device.
Important information
K5902146 (451920612625) /04 Eonis 37