EN ISO 11607-2in-force
EN ISO 11607-2:2020 — Packaging for terminally sterilized medical devices - Part 2: Validation requirements
EN ISO 11607-2:2020
Applies from 2011-01-01
Summary
EU MDR harmonised standard EN ISO 11607-2:2020: Packaging for terminally sterilized medical devices - Part 2: Validation requirements.
Scope
MDR (Regulation (EU) 2017/745) harmonised standard — Packaging for terminally sterilized medical devices - Part 2: Validation requirements.
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