Division 3.2 Products not covered by these Guidelines
United Kingdom
These Guidelines do not cover:
- (a)
Products that are covered by specific and equivalent notification mechanisms established by other EU legislation, notably:
- (i)
food and feed and other products covered by Regulation (EC) No 178/2002 of the European Parliament and of the Councilf1;
- (ii)
- (iii)
medical devices covered by Regulation (EU) 2017/745 of the European Parliament and of the Councilf4;
- (iv)
active implantable medical devices covered by Council Directive 90/385/EECf5.
- (i)
- (b)
Products that are not covered by the definition of a ‘product’ as laid down in Article 2(a) of the GPSD, notably:
- (i)
second-hand products or products supplied as antiques or as products to be repaired or reconditioned prior to being used, provided that the supplier clearly informs the person to whom he supplies the product to that effect (Article 2(a) of the GPSD);
- (ii)
equipment used or operated by a professional service provider to supply a service, e.g. equipment on which consumers ride or travel and equipment which is operated by a service provider and not by the consumer (recital 9 of the GPSD);
- (i)
- (c)
Products which do not enter into the definition of product contained in Article 15(4) of Regulation (EC) No 765/2008.
Annotations
Footnotes
- f1
-
Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (OJ L 31, 1.2.2002, p. 1).
- f2
-
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use (OJ L 311, 28.11.2001, p. 67).
- f3
-
Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products (OJ L 311, 28.11.2001, p. 1).
- f4
-
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (OJ L 117, 5.5.2017, p. 1).
- f5
-
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (OJ L 189, 20.7.1990, p. 17).