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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: 22/04/2020 - Created by GROW.R.2.DIR - Publication date: n/a - Last update: 24/04/2020
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Last update: 24/04/2020 | top