
7
Aurical Otocam 300 video otoscope standards and
safety
This manual contains information and warnings, which must be followed to ensure the safe performance of the devices and
software covered by this manual. Local government rules and regulations, if applicable, should also be followed at all times.
When the Video Otoscopy module is used in conjunction with a device (including devices other than those produced by
Otometrics), make sure that all information and warnings in the documentation of the device are followed.
ISO 15223-1
Symbol 5.1.1
Manufacturer
Indicates the medical device manufacturer, as defined in EU Directives 90/385/EEC, 93/42/EEC
and 98/79/EC.
ISO 15223-1
Symbol 5.1.3
Date of manufacture.
Indicates the date when the medical device was manufactured.
ISO 15223-1
Symbol 5.1.7
Serial number
Indicates the manufacturer’s serial number so that a specific medical device can be identified.
ISO 15223-1
Symbol 5.1.6
Catalog/product number
Indicates the manufacturer’s catalogue number so that the medical device can be identified.
IEC 60601-1
Table D.1 #20
Type BF applied part
Complies with Type BF requirements of IEC 60601-1.
93/42/EEC
CE marking of conformity
Certification mark that indicates conformity with applicable regulations and directives for the
European Economic Area.
Medical device
ISO 15223-1
Symbol 5.1.5
Use-by date
Indicates the date after which the medical device is not to be used.
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Aurical Otocam 300
7 Aurical Otocam 300 video otoscope standards and safety