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Regulation (EC) No 765/2008 of the European Parliament and of the CouncilDangos y teitl llawn

Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 (Text with EEA relevance)

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Regulation (EC) No 765/2008 of the European Parliament and of the Council, CHAPTER I is up to date with all changes known to be in force on or before 20 January 2026. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations. Help about Changes to Legislation

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CHAPTER IU.K.GENERAL PROVISIONS

Article 1U.K.Subject matter and scope

1.This Regulation lays down rules on the organisation and operation of accreditation of conformity assessment bodies performing conformity assessment activities.

2.This Regulation provides a framework for the market surveillance of products to ensure that those products fulfil requirements providing a high level of protection of public interests, such as health and safety in general, health and safety at the workplace, the protection of consumers, protection of the environment and security.

3.This Regulation provides a framework for controls on products [F1entering the market of Great Britain].

[F24.This Regulation provides the requirements as to the form of the UK marking.]

Article 2U.K.Definitions

For the purposes of this Regulation the following definitions F3... apply:

1.

‘making available on the market’ [F4means] any supply of a product for distribution, consumption or use on the [F5market of Great Britain] in the course of a commercial activity, whether in return for payment or free of charge [F6and related expressions must be construed accordingly];

2.

‘placing on the market’ [F4means] the first making available of a product on the [F7market of Great Britain ][F8and related expressions must be construed accordingly];

3.

‘manufacturer’ [F4means] 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.

[F9authorised representative” means a person who—

(a)

is established in the United Kingdom; and

(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.

[F10importer” means any person established in the United Kingdom who places a product from a country outside of the United Kingdom on the market;]

6.

‘distributor’ [F11means] 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.

‘economic operators’ [F12means] the manufacturer, the authorised representative, the importer and the distributor;

8.

F13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9.

F13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

10.

[F14accreditation” 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.

[F15UK national accreditation body” means the body appointed by the Secretary of State in accordance with Article 4;]

12.

‘conformity assessment’ [F16means] the process demonstrating whether specified requirements relating to a product, process, service, system, person or body have been fulfilled;

13.

‘conformity assessment body’ [F16means] a body that performs conformity assessment activities including calibration, testing, certification and inspection;

14.

‘recall’ [F16means] any measure aimed at achieving the return of a product that has already been made available to the end user;

15.

‘withdrawal’ [F16means] any measure aimed at preventing a product in the supply chain from being made available on the market;

16.

F17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

17.

‘market surveillance’ [F18means] the activities carried out and measures taken by public authorities to ensure that products comply with the requirements set out in [F19any relevant enactment] and do not endanger health, safety or any other aspect of public interest protection;

18.

[F20market surveillance authority” means an authority responsible for carrying out market surveillance in the United Kingdom;]

19.

[F21the free circulation procedure” means the procedure set out in Schedule 1 to the Taxation (Cross-border Trade) Act 2018;]

20.

[F22conformity 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.

[F23relevant enactment” means any [F24assimilated] law, as it applies in Great Britain, derived from an EU instrument harmonising the conditions for the marketing of products in the EU;]

22.

[F25UK marking” means the marking in the form set out in Annex 2.]

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