Art. 24 Involvement of a designated body
1 When a designated body is involved, all the information necessary for the conformity assessment must be made available to it. 2 Manufacturers must not apply to more than one designated body in Switzerland or a contracting state to conduct a conformity assessment procedure for the same product. 3 Any natural or legal person who applies to a designated body must inform that body whether an application to a different designated body in Switzerland or a contracting state has been withdrawn before a decision was issued or rejected by a different designated body in Switzerland or a contracting state. 4 If a manufacturer withdraws its application to have a conformity assessment procedure conducted before the designated body has issued its decision on the assessment, the designated body in question will notify Swissmedic and the other designated bodies. 5 The information required in paragraph 4 must be supplied exclusively via Eudamed. 6 Where a manufacturer voluntarily changes designated body, it must comply with the requirements of Article 58 EU-MDR38. 38 See the footnote to Art. 4 para. 1 let. f. |