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About This Item

 

Full Description

ISO 17664:2017 specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection and/or sterilization to ensure that the device is safe and effective for its intended use.

This includes information for processing prior to use or reuse of the medical device. The provisions of this document are applicable to medical devices that are intended for invasive or other direct or indirect patient contact.
 

Document History

  1. ISO 17664-1:2021


    Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices

    • Most Recent
  2. ISO 17664:2017

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    Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices

    • Historical Version
  3. ISO 17664:2004


    Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices

    • Historical Version