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Division 4 Assessment of the technical documentation applicable to class III devices and to the class IIb devices referred to in the second subparagraph of Article 52(4)F1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 4.1Division 4.1
  2. 4.2Division 4.2
  3. 4.3Division 4.3
  4. 4.4Division 4.4
  5. 4.5Division 4.5
  6. 4.6Division 4.6
  7. 4.7Division 4.7
  8. 4.8Division 4.8
  9. 4.9Division 4.9
  10. 4.10Division 4.10

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))