{
  "url": "https://openlegislation.uk/draft-medical-devices-amendment-etc-eu-exit-regulations-2020/schedule-2/paragraph-20",
  "json_url": "https://openlegislation.uk/draft-medical-devices-amendment-etc-eu-exit-regulations-2020/schedule-2/paragraph-20.json",
  "legislation": "ukdsi/2020/9780348214956",
  "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",
  "path": "schedule/2/paragraph/20",
  "kind": "paragraph",
  "number": "20",
  "heading": "Insertion of regulation 4(7D)",
  "text": "After regulation 4(7C) insert—\n“(7D) In regulation 16 (procedures for general medical devices for clinical investigation)—\n(a) for “his authorised representative” each time those words occur, substitute “their UK responsible person”;\n(b) in paragraph (1), for “the United Kingdom” substitute “Great Britain”;\n(c) in paragraph (2)—\n(i) for “CE marking” substitute “UK marking”;\n(ii) for “CE marked” substitute “UK marked”;\n(d) in paragraph (4) for “or authorised representative” substitute “or UK responsible person”;\n(e) in paragraph (11) for “single authorised representative” substitute “single UK responsible person”.”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/ukdsi/2020/9780348214956/schedule/2/paragraph/20",
    "retrieved_at": "2026-10-30T14:48:13.546182+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."
}