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3. Application for supervised product checks at random intervals

Before placing PPE on the market, the manufacturer shall lodge an application for supervised product checks at random intervals with a single notified body of his choice. The application shall include the following: the name and address of the manufacturer and, if the application is lodged by the authorised representative, his name and address; a written declaration that the same application has not been lodged with any other notified body; the identification of the PPE concerned. Where the chosen body is not the body that has carried out the EU type-examination, the application shall also include the following: the technical documentation described in Annex III; a copy of the EU type-examination certificate.

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Source: EUR-Lex (Cellar) · retrieved 2026-11-01 · Text as adopted (Official Journal); later amendments are not incorporated in this text.