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Section 19

CE marking

(1) Before a product whose conformity with the accessibility requirements of the statutory instrument to be issued under section 3(2) has been demonstrated by the conformity assessment procedure under Annex 2 is placed on the market, it must be affixed with the CE marking, in accordance with subsection (2), by the manufacturer or, where the task has been assigned to it, its authorised representative.
(2) The CE marking must be affixed visibly, legibly and indelibly to the product or to its data plate. Where the nature of the product does not allow or justify this, it must be affixed to the packaging and to the accompanying documents.
(3) The CE marking is subject to the general principles set out in Article 30 of 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 (OJ L 218, 13.8.2008, p. 30; OJ L 169, 25.6.2019, p. 1), as amended from time to time.

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