Division 18 Conclusion of this assessment:
United Kingdom
Based on the evaluation of data and the assessment process it is our preliminary decision that the application meets the requirements of conformity with
and 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(b)(ii)
- F2
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(b)(iii)
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)
Notes on Division
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(b)(i)