MDCG 2020-6 Regulation (EU) 2017/745: Clinical evidence needed for medical devices previously CE marked under Directives 93/42/EEC or 90/385/EEC. A guide for manufacturers and notified bodies
Document date: Wed Apr 22 00:00:00 CEST 2020
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- Last update: Fri Apr 24 07:33:41 CEST 2020
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