Barco AMM215WTD User Manual page 39

Important information
Indicates the device meets the requirements of the applicable EC directives/
regulations.
Indicates compliance with Part 15 of the FCC rules (Class A or Class B).
Medical equipment is in accordance with UL 60601-1 and CAN/CSA C22.2 No.
601.1 in regards to electric shock, fire and mechanical hazards
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 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 legal manufacturer.
Indicates the manufacturing date.
Indicates the entity importing the medical device into the locale.
Indicates this is a Medical Device.
MD
Indicates the device serial number.
SN
Indicates the device part number or catalogue number.
REF
Indicates the Unique Device Identifier.
UDI
Warning: dangerous voltage
Caution
Consult the Instructions For Use.
R5912860 /13 AMM215WTD 39