|
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 simultaneously apply to more than one designated body in Switzerland or a contracting state to carry out 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inform that body whether an application to a different designated body in Switzerland or a contracting state has been withdrawn before a decision was issued or rejected by a different designated body in Switzerland or a contracting state. 4 If a manufacturer withdraws its application to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 carried out before the designated body has issued its decision on the assessment, the designated body in question shall notify Swissmedic and the other designated bodies. 5 ...62 6 Where a manufacturer voluntarily changes the designated body, it must comply with the requirements of Article 58 EU-MDR63. 62 Repealed by Annex 5 No 1 of the O of 4 May 2022 on In Vitro Diagnostic Medical Devices, with effect from 26 May 2022 (AS 2022 291). 63 See the footnote to Art. 4 para. 1 let. f. |