Orascoptic SPARK Serie Instrucciones De Uso Y Mantenimiento página 12

Symbol Symbol Title
Medical Device
Catalogue Number
Serial Number
Batch Code
Unique Device Identifier
European Conformity
UK Conformity
Canadian Standards Association
Authorized Representative
EC REP
in the European Community
CH REP
Swiss Authorized Representative
Authorized Representative
UK RP
in United Kingdom
Full explanation of symbols as used on Kerr packaging located at: http://www.kerrdental.com/symbols-glossary
12
INSTRUCTIONS FOR USE AND CARE
™ ™
Orascoptic Spark
Symbol Glossary
Explanatory Text
Indicates the medical device manufacturer.
Indicates the manufacturer's catalogue number so that the medical device can be identified.
Indicates the manufacturer's serial number so that a specific medical device can be identified.
Indicates the manufacturer's batch code so that the batch or lot can be identified.
Indicates a carrier that contains unique device identifier information.
European conformity (CE) mark for Class I medical devices.
UK Conformity (UKCA) mark for Class I medical devices (non-sterile, no measuring function, and not resusable surgical instrument).
Indicates the device has been tested against applicable North American standards requirements.
Indicates the authorized representative in the European Community.
Indicates the authorized representative based in Switzerland.
Indicates the authorized representative based in United Kingdom.
Series Headlight