Regulatory guidance
Guidance on transitional provisions for consultations of authorities on devices incorporating a substance which may be considered a medicinal product and which has action ancillary to that of the device, as well as on devices manufactured using TSE susceptible animal tissues
Published Jun 1, 2020
Reference
MDCG 2020-12
Source
MDCG
Topic
Notified bodies
Published
Jun 1, 2020
Languages
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
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