Indicates the need for the user to consult the instructions for use.Ī.16 Example of use of symbol 5.4.3, “Consult instructions for use” for an electronic instruction for use (eIFU)
Indicates a medical device that is intended for one single use only. Indicates that there are potential biological risks associated with the medical device. Indicates the range of atmospheric pressure to which the medical device can be safely exposed. Indicates the range of humidity to which the medical device can be safely exposed. Indicates the temperature limits to which the medical device can be safely exposed. Indicates the upper limit of temperature to which the medical device can be safely exposed. Indicates the lower limit of temperature to which the medical device can be safely exposed. Indicates a medical device that needs to be protected from moisture. NOTE: This symbol can also mean “Keep away from heat”. Indicates a medical device that needs protection from light sources. Indicates a medical device that can be broken or damaged if not handled carefully. Indicates a single sterile barrier system with protective packaging outside. Single sterile barrier system with protective packaging outside Indicates a single sterile barrier system with protective packaging inside. Single sterile barrier system with protective packaging inside Indicates a single sterile barrier system. NOTE 2: Medical device contains a sterile fluid path that has been sterilized using irradiation. NOTE 1: Medical device contains a sterile fluid path that has been sterilized using ethylene oxide Indicates the presence of a sterile fluid path within the medical device in cases when other parts of the medical device, including the exterior, might not be supplied sterile.Ī.12 Examples of use of symbol 5.2.9 for “Sterile fluid path” NOTE 1: This symbol can also mean “Do not use if the product sterile barrier system or its packaging is compromised”. Indicates a medical device that should not be used if the package has been damaged or opened. Indicates a medical device that has not been subjected to a sterilization process.ĭo not use if package is damaged and consult instructions for use Indicates a medical device that is not to be resterilized. Indicates a medical device that has been sterilized using steam or dry heat. Indicates a medical device that has been sterilized using irradiation. Indicates a medical device that has been sterilized using ethylene oxide. Indicates a medical device that has been manufactured using accepted aseptic techniques. Sterilized using aseptic processing techniques Indicates a medical device that has been subjected to a sterilization process. Indicates the model number or type number of a product
Push switch symbol iso serial number#
Indicates the manufacturer’s serial number so that a specific medical device can be identified. Indicates the entity importing the medical device into the locale. NOTE: Synonyms for “catalog number” are “commercial product name”, “commercial product code”, stock keeping unit, “reference number” and “reorder number”. Indicates the manufacturer’s catalogue number so that the medical device can be identified.
Push switch symbol iso code#
Indicates the manufacturer’s batch code so that the batch or lot can be identified.
NOTE: Synonyms for “use-by date” are “use by”, “expiry date” and “expiration date”. Indicates the date after which the medical device is not to be used. Indicates the date when the medical device was manufactured. Indicates the authorized representative in the European Community / European Union. Indicates the medical device manufacturer.Īuthorized representative in the European Community Medical Device ID Cards - Pacemaker, ICD, & CRT devices.Transcatheter Aortic Valve Replacement (TAVR).Cardiac Resynchronization Therapy (CRT) Devices.
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