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Division PART B PRODUCT VERIFICATIONF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 11Division 11
  2. 12Division 12
  3. 13Division 13
  4. 14Division 14
  5. 15Verification by examination and testing of every product
  6. 16Division 16
  7. 17Administrative provisions
  8. 18Application to class IIa devices

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))