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80-0078-00-MO-RevD 2018-08-02 SunTech CT50 User Manual | 12
Symbol
Symbol Title
Symbol Description
Standard/
Source
Date of Manufacture
Indicates the date when the medical device was
manufactured.
ISO 7000-2497
Manufacturer
Indicates the medical device manufacturer, as defined in EU
Directives 90/385/ EEC, 93/42/EEC and 98/79/EC.
ISO 7000-3082
Catalogue number
Indicates the manufacturer’s catalogue number so that the
medical device can be identified.
ISO 7000-2493
Batch code
Indicates the manufacturer’s batch code so that the batch or
lot can be identified.
ISO 7000-2492
Serial number
Serial number
ISO 7000-2498
Temperature limit
Indicates the temperature limits to which the medical device
can be safely exposed.
ISO 7000-0632
Humidity limitation
Indicates the range of humidity to which the medical device
can be safely exposed.
ISO 7000-2620
Atmospheric pressure
limitation
Indicates the range of atmospheric pressure to which the
medical device can be safely exposed.
ISO 7000-2621
CE mark:
Product meets the Medical Device Directive and is CE marked
to indicate conformance.
EU Directive
Disposal
Symbol for the marking of electrical and electronics devices
according to Directive 2002/96/EC.
WEEE Directive
Authorized
representative in the
European Community
Indicates the authorized representative in the European
Community.
EU Directive
Alarm Pause
Indicates the alarm is paused.
IEC 60417-5319
Alarm Reset
Identifies the control for alarm reset.
IEC 60417-5309
Active Alarm
Indicates an alarm condition.
IEC 60417-5307
12


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