EN ISO 10993-9in-force
EN ISO 10993-9:2009 — Biological evaluation of medical devices - Part 9: Identification of potential degradation products
EN ISO 10993-9:2009
Applies from 2011-01-01
Summary
EU MDR harmonised standard EN ISO 10993-9:2009: Biological evaluation of medical devices - Part 9: Identification of potential degradation products.
Scope
MDR (Regulation (EU) 2017/745) harmonised standard — Biological evaluation of medical devices - Part 9: Identification of potential degradation products.
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