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 - 2021 EDITION - 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.

To find similar documents by classification:

11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)

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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)