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Chapter IV NOTIFIED BODIESF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 35Authorities responsible for notified bodies
  2. 36Requirements relating to notified bodies
  3. 37Subsidiaries and subcontracting
  4. 38Application by conformity assessment bodies for designation
  5. 39Assessment of the application
  6. 40Nomination of experts for joint assessment of applications for notification
  7. 41Language requirements
  8. 42Designation and notification procedure
  9. 43Identification number and list of notified bodies
  10. 44Monitoring and re-assessment of notified bodies
  11. 45Review of notified body assessment of technical documentation and clinical evaluation documentation
  12. 46Changes to designations and notifications
  13. 47Challenge to the competence of notified bodies
  14. 48Peer review and exchange of experience between authorities responsible for notified bodies
  15. 49Coordination of notified bodies
  16. 50List of standard fees

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))