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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.
IS 13252 (Part 1)
Indicates the device is approved according to the BIS regulations.
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.
Indicates the DisplayPort connectors on the device.
Indicates the legal manufacturer.
Indicates the manufacturing date.
yy
Indicates the temperature limitations
xx
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
5:
Values for xx and yy can be found in the technical specifications paragraph.
5
for the device to safely operate within specs.
K5902105 (451920611795) /04
Important information
MDSC-2232
67
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