anx_IV__cpt_3__text_3

the Directive references, name and address of the manufacturer or its authorised representative established within the Community (give trade name and full address; in the case of the authorised representative, also give the trade name of the manufacturer), description of interoperability constituent (make, type, etc.), description of the procedure followed in order to declare conformity or suitability for use (Article 13), all the relevant descriptions met by the interoperability constituent and, in particular, its conditions of use, name and address of the notified body or bodies involved in the procedure followed in respect of conformity or suitability for use and date of examination certificate together with, where appropriate, the duration and conditions of validity of the certificate, where appropriate, reference to the European specifications, identification of the signatory empowered to enter into commitments on behalf of the manufacturer or of the manufacturer's authorised representative established within the Community.

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.