Regulatory guidance
Regulation (EU) 2017/746 - application of IVDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2022 in accordance with Directive 98/79/EC
Published May 1, 2022
Reference
MDCG 2022-8
Source
MDCG
Topic
In Vitro Diagnostic medical devices (IVD)
Published
May 1, 2022
Languages
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
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