marsden PT-700, Руководство пользователя

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Explanation of Graphic Symbols
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
19 : Year in which conformity verification was performed and the CE
label was applied. (ex: 19=2019)
0122 : Refers to Notified Body for metrology
Device complies with UK Regulation.
M : Non-Automatic Weighing Instruments Regulations 2016.
21 : Year in which conformity verification was performed and the CE
label was applied. (ex: 21=2021)
0120 : Refers to the Approved Body for metrology