Indicates the manufacturer's batch code so that the batch or lot can be identified. ISO 15223, 5.1.5
Indicates the need for the user to consult the instructions for use for important cautionary information such as warnings and precautions that cannot, for a variety of reasons, be presented on the medical device itself. Source: ISO 15223, 5.4.4
Indicates the need for the user to consult the instructions for use. Source: ISO 15223, 5.4.3
Indicates the presence of natural rubber or dry natural rubber latex as a material of construction within the medical device or the packaging of a medical device. Source: ISO 15223, 5.4.5
Indicates natural rubber or dry natural rubber latex is not present as a material of construction within the medical device or the packaging of a medical device. Source: ISO 15223, 5.4.5 and Annex B
Indicates a medical device that has been sterilized using ethylene oxide. Source: ISO 15223, 5.2.3
Indicates a medical device that has been sterilized using irradiation. Source: ISO 15223, 5.2.4
Indicates the date after which the medical device is not to be used. Source: ISO 15223, 5.1.4
Indicates a medical device that is intended for one use or for use on a single patient during a single procedure. Source: ISO 15223, 5.4.2