14
3.9
About Labels in Rating plate
Explanations of labels in rating plate are described in following table.
CE mark for Europe
98/79/EC (IVD Directive)
This instrument has been tested to and complies with
standards IEC61010-
1 Ed.3 (2010), “Safety
Requirements for Electrical Equipment for
Measurement, Control and Laboratory Use
‐
Part 1:
General Requirements;
”
IEC61010-2-
101(2015), “Safety requirements for
electrical equipment for measurement, control, and
laboratory use
‐
Part 2
‐
101: Particular
requirements for in vitro diagnostic (IVD) medical
equipment.”
IEC61326-
1 (2013), “Electrical equipment for
measurement, Control and laboratory use EMC
requirements
–
Part1: General requirements.”
IEC61326-2-
6 (2013), “Electrical equipment for
measurement, Control and laboratory use EMC
requirements
–
Part2-6: Particular requirements in
vitro diagnostic (IVD) medical equipment.”
UL listing mark for Canada and the USA
This instrument has been tested to and complies with
standards UL 61010
‐
1 Ed.3 (2012) and CSA-C22.2
No.61010-1-
12 Ed3.(2012), “Safety Requirements for
Electrical Equipment for Measurement, Control and
Laboratory Use, Part 1: General Requirements.”
WEEE mark for Europe
Serial number
Legal Manufacturer
Authorized Representative in the European Community
