Chapter VIII COOPERATION BETWEEN MEMBER STATES, MEDICAL DEVICE COORDINATION GROUP, EXPERT LABORATORIES, EXPERT PANELS AND DEVICE REGISTERSF1
United Kingdom Repealed
- 101Competent authorities
- 102Cooperation
- 103Medical Device Coordination Group
- 104Support by the Commission
- 105Tasks of the MDCG
- 106Provision of scientific, technical and clinical opinions and advice
- 107Conflict of interests
- 108Device registers and databanks
Annotations
Textual amendments
- F1
Regulation revoked (31.12.2020) by The Medical Devices Regulations 2002 (S.I. 2002/618), reg. 4O (with savings and transitional provisions for N.I. in reg. 3ZA) (as amended by S.I. 2019/791, regs. 1(1), 3(7) and by S.I. 2020/1478, regs. 1(3), Sch. 2 para. 2; and as amended (27.7.2021) by The Medical Devices (Northern Ireland Protocol) Regulations 2021 (S.I. 2021/905), regs. 1(2), 4, 32); 2020 c. 1, Sch. 5 para. 1(1))