CAN/CSA-ISO/TS 17665-3:2017 Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization
This part of ISO 17665 provides guidance about the attributes of a medical device to be considered by
the user when assigning a medical device to a product family for the purpose of identifying and aligning
it to a processing category for a specific moist heat sterilization process.
NOTE While this part of ISO 17665 is applicable to health care facilities, it may be used by a manufacturer of
a sterile medical device and/or whenever information on reprocessing is required (see ISO 17664).
CAN/CSA-ISO/TS 17665-3:2017 history
1970CAN/CSA-ISO/TS 17665-3:2017 Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization