BurnTec®. First aid dressings for burns and skin injuries
The BurnTec brochure
The North American Rescue Brochure
Indicates the manufacturer’s batch code so that the batch or lot can be identified.
Indicates the date after which the medical device is not to be used.
Indicates the medical device manufacturer, asdefined in EU Directives: 90/385/EEC, 93/42/EEC and 98/79/EC.
Do not re-use
Indicates a medical device that is intended for one use, or for use on a single patient during a single procedure.
Do not resterilize
Indicates a madical device that is not to be resterilized.
Sterilized using irradiation
Indicates a medical device that has been sterilized using irradiation.
Indicates a medical device that needs to be protected from moisture.
Indicates the temperature limits to which the medical device can be safely exposed.
Do not use if package is damaged
Indicates a medical device that should not be used if the package has been damaged or opened.
It means that after use, the packaging should be discarded in a suitable container so that it does not endanger or litter the environment.
Indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA)
Identify the material from which an item is made, to facilitate easier recycling or other reprocessing. (kompozyt, polietylen, aluminium)