The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024
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Change 1
6 Saving provision
(1) The modifications made by Schedule 2A continue to apply, as if they had not been amended by regulation 5, to relevant devices— (a) put into service by the manufacturer, or (b) placed on the market, in accordance with Parts 2, 3 or 4 before the date on which these Regulations came into force. (2) In this regulation, “relevant device” means a device that is a “relevant device” for the purposes of Part 2, 3 or 4 of the Medical Devices Regulations 2002.
6 Saving provision
(1) The modifications made by Schedule 2A continue to apply, as if they had not been amended by regulation 5, to relevant devices— (a) put into service by the manufacturer, or (b) placed on the market, in accordance with Parts 2, 3 or 4 before the date on which these Regulations came into force. (2) In this regulation, “relevant device” means a device that is a “relevant device” for the purposes of Part 2, 3 or 4 of the Medical Devices Regulations 2002.
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