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Swissmedic's activities are based on the Law on Therapeutic Products. . importers and authorised representatives which are located in Switzerland or .Switzerland: Import of Medical Devices from the EEA into .. Jun 17, 2021 — appoint an authorized representative in Switzerland for all devices placed on the Swiss market after 26 May 2021, (i) by 31 December 2021 .Authorized Representative & Importer. Swiss/EU Authorized Representative and Importer . Registration of manufacturers, authorized representatives and importers (Art.55 MedDO, Art. 48 IvDO).SWISS FADP - Appoint a DPR. if you want to sell your medical devices in Switzerland but do not have a . to appoint an Authorized Representative, also referred to as Swiss Rep or AR.Competent Authority, Notified Body .. Jul 27, 2021 — EU National Competent Authorities ; Sweden, Medical Products Agency ; Switzerland, Swiss Agency for Therapeutic Products, Medical Devices ; Turkey .EC-REP for Swiss and British Manufacturers. EC-REP: Authorised representative under MDD, MDR, IVDD, IVDR. Because of the importance of that role of the authorized representative, the MDR and IVDR have .GMB Services – Swiss Authorised Representative. Foreign medical devices manufacturers must appoint a Swiss Authorized Representative to place their products on the Swiss market. As a Swiss medical device .Authorised representative. This ordinance provides that Swiss Manufacturers must designate a European Authorized Representative (or Authorized Representative) to export their devices .List of European Authorised Representative Companies .. Dec 8, 2020 — List of EU Authorised Representative companies offering AR services to Amazon sellers and cross-border e-commerce companies.EC-REP CH-REP UK-RP Services from one Source. Unique EC-REP and CH-REP with ONE address. . CH and EU Authorised Representative; UK Responsible Person. . Swiss Authorised Representative.Switzerland Register. Swissmedic is responsible for medical device regulation in Switzerland. . Only one local authorized representative can be appointed for a product category .EU MDR and its impact on Swiss - EU relations. Together with the obligation to mandate a Swiss Authorised Representative, manufacturers of medical devices who want to sell in Switzerland must respect .Switzerland – EU: MRA and Swiss authorised representative. Switzerland – EU: MRA and Swiss authorised representative. The agreement 0.946.526.81 on the mutual recognition of conformity assessment (MRA) has made .