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Chapter IV NOTIFIED BODIESF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 31Authorities responsible for notified bodies
  2. 32Requirements relating to notified bodies
  3. 33Subsidiaries and subcontracting
  4. 34Application by conformity assessment bodies for designation
  5. 35Assessment of the application
  6. 36Nomination of experts for joint assessment of applications for notification
  7. 37Language requirements
  8. 38Designation and notification procedure
  9. 39Identification number and list of notified bodies
  10. 40Monitoring and re-assessment of notified bodies
  11. 41Review of notified body assessment of technical documentation and performance evaluation documentation
  12. 42Changes to designations and notifications
  13. 43Challenge to the competence of notified bodies
  14. 44Peer review and exchange of experience between authorities responsible for notified bodies
  15. 45Coordination of notified bodies
  16. 46List of standard fees

Annotations

Textual amendments

F1

Regulation revoked (31.12.2020) by The Medical Devices Regulations 2002 (S.I. 2002/618), reg. 4P (as inserted by S.I. 2019/791, regs. 1(1), 3(7) (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 paras. 2, 9(m)); 2020 c. 1, Sch. 5 para. 1(1))