2
Explanation of Graphic Symbols on Label/Packaging
Caution, consult
accompanying documents
before use
Separate collection for
waste of electrical and
electronic equipment,
in accordance with
Directive 2002/96/EC
Manufacturer of medical
device
Manufacturing year of
medical device
Carefully read user manual
before installation and
usage, and follow
instructions for use.
Medical electrical
equipment with Type B
applied part
Device catalogue number
Authorized
representative in the
European Community
Manufacturer's batch or lot
number
Device is a medical
device
Serial number
Unique Device Identifier
Device conforms to 93/42/EEC as amended
by 2007/47/EC Medical Device Directive. Four
digit number refers to Notified Body.
Device complies with International
Organization of Legal Metrology (Class III)
requirements (verified models only)
Device complies with EC directives (verified
models only)
M
: Conformity label in compliance with
Directive 2014/31/EU for non-automatic
weighing instruments
18
: Year in which conformity verification was
performed and the CE label was applied. (ex:
18=2018)
0122
: Refers to Notified Body for metrology
Summary of Contents for MS5810
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