Medical device contains a sterile fluid path that has been sterilized using ethylene oxide.Įxamples of use of symbol 5.2.9 for “Sterile fluid path”. 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 sterileĮxamples of use of symbol 5.2.9 for “Sterile fluid path”. Indicates a medical device that has not been subjected to a sterilization process Indicates a medical device that is not to be resterilized To indicate that the device is provided sterile and 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 To identify the country of manufacture of products
#TRASH X SYMBOL SERIAL NUMBER#
Indicates the manufacturer's serial number so that a specific medical device can be identified Indicates the manufacturer's catalog number so that the medical device can be identified Model Name, 12 x 18 High Intensity Prismatic Aluminum Sign, 12 x 18 Reflective Aluminum Sign, 12 x 18 Steel Sign, 18 x 24 High Intensity Prismatic. Synonyms for “batch code” are “lot number”, “lot code” and “batch number”.
#TRASH X SYMBOL CODE#
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 date when the medical device was manufactured
It is represented with a 'chasing arrows' symbol surrounding a a number between 1 and 7 that defines the resin used. Indicates the authorized representative in the European Community / European Union Plastic resin codes These identify the type of plastic resin used to make the item by providing a 'Resin Identification Code'. Indicates the medical device manufacturerĪuthorized Representative in the European Community/ European Union Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements.
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