Article 2 Definitions

For the purposes of this Regulation the following definitions F1... apply:

1. 1..

   ‘making available on the market’ F2means any supply of a product for distribution, consumption or use on the F3market of Great Britain in the course of a commercial activity, whether in return for payment or free of charge F4and related expressions must be construed accordingly;

2. 2..

   ‘placing on the market’ means the first making available of a product on the F5market of Great Britain F6and related expressions must be construed accordingly;

3. 3..

   ‘manufacturer’ means any natural or legal person who manufactures a product or has a product designed or manufactured, and markets that product under his name or trademark;

4. 4..

   F7“authorised representative” means a person who—

   1. (a)

      is established in the United Kingdom; and

   2. (b)

      has received a written mandate from a manufacturer to act on that manufacturer's behalf in relation to specified task with regard to the manufacturer's obligation under any relevant enactment;

5. 5..

   F8“importer” means any person established in the United Kingdom who places a product from a country outside of the United Kingdom on the market;

6. 6..

   ‘distributor’ F9means any natural or legal person in the supply chain, other than the manufacturer or the importer, who makes a product available on the market;

7. 7..

   ‘economic operators’ F10means the manufacturer, the authorised representative, the importer and the distributor;

8. 8..

   F11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9. 9..

   . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

10. 10..

    F12“accreditation” means an attestation by a national accreditation body conveying formal recognition that a conformity assessment body is competent to carry out a specific conformity assessment activity;

11. 11..

    F13“UK national accreditation body” means the body appointed by the Secretary of State in accordance with Article 4;

12. 12..

    ‘conformity assessment’ F14means the process demonstrating whether specified requirements relating to a product, process, service, system, person or body have been fulfilled;

13. 13..

    ‘conformity assessment body’ means a body that performs conformity assessment activities including calibration, testing, certification and inspection;

14. 14..

    ‘recall’ means any measure aimed at achieving the return of a product that has already been made available to the end user;

15. 15..

    ‘withdrawal’ means any measure aimed at preventing a product in the supply chain from being made available on the market;

16. 16..

    F15. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

17. 17..

    ‘market surveillance’ F16means the activities carried out and measures taken by public authorities to ensure that products comply with the requirements set out in F17any relevant enactment and do not endanger health, safety or any other aspect of public interest protection;

18. 18..

    F18“market surveillance authority” means an authority responsible for carrying out market surveillance in the United Kingdom;

19. 19..

    F19“the free circulation procedure” means the procedure set out in Schedule 1 to the Taxation (Cross-border Trade) Act 2018;

20. 20..

    F20“conformity marking” means a marking, such as the UK marking, by which the manufacturer indicates that a product is in conformity with the applicable requirements of any enactment providing for the affixing such a marking;

21. 21..

    F21“relevant enactment” means any F22assimilated law, as it applies in Great Britain, derived from an EU instrument harmonising the conditions for the marketing of products in the EU;

22. 22.

    F23“UK marking” means the marking in the form set out in Annex 2.