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About This Item

 

Full Description

This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i.e. a medical device that enters normally sterile parts of the human body or a medical device that comes into contact with mucous membranes or non-intact skin) or medical devices that are intended to be sterilized.

All current amendments available at time of purchase are included with the purchase of this document.

 

Document History

  1. BS EN ISO 17664-1:2021

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

    • Most Recent
  2. BS EN ISO 17664:2017


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

    • Historical Version
  3. BS EN ISO 17664:2004


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

    • Historical Version