Indicates the medical device manufacturer, as defined in EU Directives 90/385/EEC, 93/42/EEC and 98/79/EC.
Ref. 5.1.1 in ISO 15223-1 and ISO 7000-3082
|Authorized Representative in the European Community
Indicates the authorized representative in the European Community.
Ref. 5.1.2 in ISO 15223-1
Indicates the date after which the medical device is not to be used.
Ref. 5.1.4 in ISO 15223-1 and ISO 7000-2607
Indicates the manufacturer’s batch code so that the batch or lot can be identified.
Ref. 5.1.5 in ISO 15223-1 and ISO 7000-2492
Indicates the manufacturer’s catalogue number so that the medical device can be identified.
Ref. 5.1.6 in ISO 15223-1 and ISO 7000-2493
Indicates a medical device was subjected to a sterilization process with ethylene oxide.
Ref. 5.2.3 in ISO 15223-1 and ISO 7000-2501
Indicates a medical device that has not been subjected to a sterilization process.
Ref. 5.2.7 in ISO 15223-1 and ISO 7000-2609
|Do not use if package is damaged.
Indicates a medical device that should not be used if the package has been damaged or opened.
Ref. 5.2.8 in ISO 15223-1 and ISO 7000-2606
|Do not reuse.|
Indicates a medical device is intended for one use, or for use on a single patient during a single procedure.
Ref 5.4.2 in ISO 15223-1 and ISO 7000-1051
|Consult instructions for use
Indicates the need for the user to consult the instructions for use.
Ref. 5.4.3 in ISO 15223-1 and ISO 7000-1641
|Quantity||CAUTION! Federal (US) law restricts this device to sale by or on order of a licensed healthcare practitioner.|
ISO 7000:2014 Graphical Symbols for Use on Equipment - Registered Symbols
ISO 15223-1:2016 Medical Devices - symbols to be Used with Medical Devices Labels, Labeling, and Information to be Supplied - Part 1: General Requirements