Summary
EU MDR harmonised standard EN 556-2:2015: Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Aseptically processed.
Scope
MDR (Regulation (EU) 2017/745) harmonised standard — Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Aseptically processed.
Expert analysis
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