{
  "url": "https://openlegislation.uk/draft-medical-devices-northern-ireland-protocol-regulations-2021/regulation-30",
  "json_url": "https://openlegislation.uk/draft-medical-devices-northern-ireland-protocol-regulations-2021/regulation-30.json",
  "legislation": "ukdsi/2021/9780348224740",
  "legislation_title": "The Medical Devices (Northern Ireland Protocol) Regulations 2021",
  "legislation_url": "https://openlegislation.uk/draft-medical-devices-northern-ireland-protocol-regulations-2021",
  "path": "regulation/30",
  "kind": "regulation",
  "number": "30",
  "heading": "Amendment of regulation 2 (interpretation)",
  "text": "In regulation 2, in paragraph (1)—\n(a) for the definition of “medical device” substitute—\n““medical device” has the meaning given in Article 2(1) of Regulation (EU) 2017/745 and includes devices intended to administer a medicinal product or which incorporate as an integral part a substance which, if used separately, would be a medicinal product and which is liable to act upon the body with action ancillary to that of the device;”;\n(b) after the definition of “Regulation 722/2012” insert—\n““Regulation (EU) 2017/745” means Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC;”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/ukdsi/2021/9780348224740/regulation/30",
    "retrieved_at": "2026-10-30T14:46:58.636532+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."
}