Orascoptic Spark Instructions D'utilisation Et D'entretien page 12

Symbol Symbol Title
Medical Device
Catalogue Number
Serial Number
Batch Code
Unique Device Identification
European Conformity
UK Conformity
Canadian Standards Association
Authorized Representative
EC REP
in the European Community
Authorized Representative
UK RP
in United Kingdom
Swiss Authorized Representative
and Importer
Distributor
Waste Stream Disposal Status
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 United Kingdom.
Indicates the authorized representative and importer based in Switzerland.
Indicates the entity distributing the medical device into the local.
Do not dispose of electronic products in the general wastestream.
Series Headlight