Division 10 Confirmation that the submitting approved body has been designated by the Secretary of State for the conformity assessment ofF1
United Kingdom
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active implantable medical devices manufactured utilising tissues of animal origin subject to Regulation (EU) No 722/2012,
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medical devices manufactured utilising tissues of animal origin subject to Regulation (EU) No 722/2012
Annotations
Textual amendments
- F1
Words in Annex 2 substituted (11.8.2021) by The Medical Devices (Amendment) (EU Exit) Regulations 2021 (S.I. 2021/873), reg. 1(1), Sch. 2 para. 16(a)(iv)
Notes on Annex II
Textual amendments
- F1
Annex 2 heading substituted (11.8.2021) by The Medical Devices (Amendment) (EU Exit) Regulations 2021 (S.I. 2021/873), reg. 1(1), Sch. 2 para. 16(a)(i)