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The Medical Devices Regulations 2002
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- UK Statutory Instruments
- 2002 No. 618
- PART VII
- Regulation 59
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This is the original version (as it was originally made).
Interpretation of Part VII
59. In this Part, unless the context otherwise requires—
“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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