Barco AMM240ED, User Manual

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R5912858 /05 AMM240ED 34
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.
MD
Indicates this is a Medical Device.
SN
Indicates the device serial number.
REF
Indicates the device part number or catalogue number.
UDI
Indicates the Unique Device Identifier.
Warning : dangerous voltage
Caution
Important information