The Medical Devices (In Vitro Diagnostic Devices etc.) (Amendment) Regulations 2024
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Change 1
24 Amendment to the Waste Electrical and Electronic Equipment Regulations 2013
In the Waste Electrical and Electronic Equipment Regulations 2013, in regulation 2 (interpretation), for the definition of “in vitro diagnostic medical device”, substitute— “in vitro diagnostic medical device” means an in vitro diagnostic device or accessory within the meaning of— regulation 2(1) of the Medical Devices Regulations 2002 in relation to England and Wales and Scotland, and Article 2 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU in relation to Northern Ireland, which is EEE;. .
24 Amendment to the Waste Electrical and Electronic Equipment Regulations 2013
In the Waste Electrical and Electronic Equipment Regulations 2013, in regulation 2 (interpretation), for the definition of “in vitro diagnostic medical device”, substitute— “in vitro diagnostic medical device” means an in vitro diagnostic device or accessory within the meaning of— regulation 2(1) of the Medical Devices Regulations 2002 in relation to England and Wales and Scotland, and Article 2 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU in relation to Northern Ireland, which is EEE;. .
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