# The Medical Devices Regulations 2002, Regulation 21: Scope of Part III

Extent: E+W+S

(1) The requirements of this Part in respect of relevant devices apply in respect of active implantable medical devices and accessories to such devices, ...
(2) Where a hazard exists, devices which are also machinery shall also meet the essential health and safety requirements set out in Part 1 of Schedule 2 to the Supply of Machinery (Safety) Regulations 2008 to the extent to which those essential health and safety requirements are more specific than the essential requirements set out in Annex I to Directive 90/385.
(3) Where an active implantable device is intended to administer a medicinal product, that device must be governed by this Part without prejudice to the provisions of the Human Medicines Regulations 2012.
(4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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Source: https://www.legislation.gov.uk/uksi/2002/618/regulation/21 (the official version)
Page: https://openlegislation.uk/medical-devices-regulations-2002/regulation-21
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.