SS-EN-ISO-17664-1 › 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 (ISO 17664-1:2021)
SS-EN-ISO-17664-1
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2021 EDITION
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CURRENT
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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. This includes information for processing prior to use or reuse of the medical device.
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Designation Name
SS-EN ISO 17664-1:2021
Revision Level
2021 EDITION
Status
Current
Publication Date
Sept. 6, 2021
Language(s)
English
Page Count
36
International Equivalent
EN ISO 17664-1:2021(IDT); ISO 17664-1:2021(IDT)