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The Medical Devices Regulations 2002

Changes over time for: Section 59

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Version Superseded: 30/04/2021

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Interpretation of Part VIIU.K.

59.  In this PartF1...—

  • “registrable device” means a device in respect of which, in accordance with the Medical Devices Directives, registration is required with the competent authorities of a Member State or (where appropriate) a State which is a Party to an Association Agreement;

  • “relevant device” means a device that is a “relevant device” for the purposes of Part II, III or IV.

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