2
Explanation of Graphic Symbols on Label/Packaging
Caution, consult
accompanying documents
before use
Authorized
representative in the
European Community
Manufacturer of medical
device
Indicates that device
conforms to
International
Organization of Legal
Metrology (Class III)
requirements
Manufacturing year of
medical device
Indicates that device
conforms to
2014/31/EU Non
Automatic Weighing
Instruments Directive.
Numerals change
according to year of
manufacture. (ex: "19"
for 2019)
Separate collection for waste
of electrical and electronic
equipment, in accordance
with Directive 2002/96/EC
Indicates that device
conforms to 93/42/EEC
as amended by
2007/47/EC Medical
Device Directive. Four
digit number refers to
Notified Body.
Device catalogue number
Indicates that device
conforms to
2014/31/EU Non
Automatic Weighing
Instruments Directive.
Four digit number refers
to Notified Body.
Manufacturer's batch or lot
number
Indicates that device is
a medical device
Serial number
Carefully read user
manual before
installation and usage,
and follow instructions
for use.
Unique Device Identifier
Medical electrical
equipment with Type B
applied part
