# The Medical Devices Regulations 2002, Regulation 30: Manufacturers etc. and conformity assessment procedures for active implantable medical devices

Extent: E+W+S

(1) A manufacturer of a relevant device or, where applicable, their UK responsible person who is required to follow, or follows or has followed a conformity assessment procedure in the Annexes referred to in regulation 27(a) shall observe the manufacturer’s obligations set out in that procedure that apply to him.
(2) A manufacturer of a relevant device or, where applicable, their UK responsible person shall, when following a conformity assessment procedure in the Annexes referred to in regulation 27(a), take account of the results of any assessment or verification operations which have been carried out ... at an intermediate stage of manufacture of the device.
(3) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(5) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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Source: https://www.legislation.gov.uk/uksi/2002/618/regulation/30 (the official version)
Page: https://openlegislation.uk/medical-devices-regulations-2002/regulation-30
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.