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Division 4.5 Conformity assessment activitiesF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 4.5.1General
  2. 4.5.2Quality management system auditing
  3. 4.5.3Product verification
  4. 4.5.4Pre-clinical evaluation assessment
  5. 4.5.5Clinical evaluation assessment
  6. 4.5.6Specific Procedures

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))