{
  "url": "https://openlegislation.uk/draft-medical-devices-amendment-etc-eu-exit-regulations-2020-ukdsi-2020-9780348213805/schedule-2/paragraph-30",
  "json_url": "https://openlegislation.uk/draft-medical-devices-amendment-etc-eu-exit-regulations-2020-ukdsi-2020-9780348213805/schedule-2/paragraph-30.json",
  "legislation": "ukdsi/2020/9780348213805",
  "legislation_title": "The Medical Devices (Amendment etc.) (EU Exit) Regulations 2020",
  "legislation_url": "https://openlegislation.uk/draft-medical-devices-amendment-etc-eu-exit-regulations-2020-ukdsi-2020-9780348213805",
  "path": "schedule/2/paragraph/30",
  "kind": "paragraph",
  "number": "30",
  "heading": "Substitution of regulation 5(6)",
  "text": "For regulation 5(6) substitute—\n“(6) In regulation 30 (manufacturers etc. and conformity assessment procedures for active implantable medical devices)—\n(a) in paragraph (3) for the opening words substitute——\n“(3) The manufacturer of a relevant device, who places devices on the market, in accordance with the procedure referred to in Article 9(2) of Directive 90/385, or, if not the manufacturer, the person placing custom-made devices on the market under that Article, must provide the Secretary of State with—”;\n(b) omit paragraphs (4) and (5).”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/ukdsi/2020/9780348213805/schedule/2/paragraph/30",
    "retrieved_at": "2026-10-30T14:48:30.666408+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}