DIN EN 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 (ISO 17664-1:2021); German version EN ISO 17664-1:2021
- Standard No.
- DIN EN ISO 17664-1:2021
- Release Date
- 2021
- Published By
- German Institute for Standardization
- Status
- Replace By
- DIN EN ISO 17664:2018
- DIN EN ISO 17664-1 E:2021-02
- Latest
- DIN EN ISO 17664:2018
- DIN EN ISO 17664-1 E:2021-02
- Scope
- 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 in
DIN EN ISO 17664-1:2021 history
- 2021 DIN EN 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 (ISO 17664-1:2021); German version EN ISO 17664-1:2021
- 2018 DIN EN ISO 17664:2018 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017); German version EN ISO 17664:2017
DIN EN 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 (ISO 17664-1:2021); German version EN ISO 17664-1:2021 was changed to DIN EN ISO 17664:2018 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017); German version EN ISO 17664:2017.
