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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
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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
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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
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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