Medical device CE marking

Obligations for authorised representatives, importers and distributors


The Medical Devices Ordinance (MedDO; SR 812.213) and the Ordinance on In Vitro Diagnostic Medical Devices (IvDO; SR 812.219) set out requirements and responsibilities for operators in the medical devices supply chain. The information sheet outlines the roles and obligations of the Swiss authorised representative, the importer and the distributor.

The information sheet can be downloaded in our library

Source: Swissmedic