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About This Item

 

Full Description

ISO/TS 17665-3:2013 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.

 

Document History

  1. ISO 17665:2024


    Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Most Recent
  2. ISO/TS 17665-3:2013

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    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

    • Historical Version
  3. ISO/TS 17665-2:2009


    Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1

    • Historical Version
  4. ISO 17665-1:2006


    Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices

    • Historical Version
  5. ISO 11134:1994


    Sterilization of health care products -- Requirements for validation and routine control -- Industrial moist heat sterilization

    • Historical Version