Schedule 1A, paragraph 14(4)

Article 3(1) is to be read as if— after point (a) there were inserted— ‘waste’ means waste within the meaning of Article 3(1) of the Waste Framework Directive, as read with Articles 5 and 6 of that Directive; ‘hazardous waste’ has the meaning given by regulation 2(1) of the Environmental Permitting (England and Wales) Regulations 2016; in point (e), “within the meaning of Article 3(1) of Directive 2008/98/EC” were omitted; in point (f)— in the words before point (i), for the words from “distance communication” to the end, there were substituted “ by means of distance communication ”; in points (i) and (ii)— for “a Member State” there were substituted “ the United Kingdom ”; for “territory of that Member State” there were substituted “ United Kingdom ”; for point (iii) there were substituted— is established in the United Kingdom and places on the market, on a professional basis, EEE from another country; or in point (iv), in the first subparagraph — for “a Member State” there were substituted “ the United Kingdom ”; “Member State or in a third” were omitted; in point (j), for “a Member State” there were substituted “ the United Kingdom ”; in point (k), for “territory of a Member State” there were substituted “ United Kingdom ”; for points (m) to (o) there were substituted— ‘medical device’ means a medical device within the meaning of regulation 2(1) or 69(1) of the Medical Devices Regulations 2002 which is EEE; ‘in vitro diagnostic medical device’ means an in vitro diagnostic medical device within the meaning of regulation 2(1) or 137 of the Medical Devices Regulations 2002 which is EEE; ‘active implantable medical device’ means an active implantable medical device within the meaning of regulation 2(1) , or the meaning determined in accordance with Schedule 9 to, of the Medical Devices Regulations 2002 which is EEE.

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Source: legislation.gov.uk · retrieved 2026-07-30