Authorized Representative service for In Vitro Diagnostic devices under IVDR 2017/746, supporting Class A through Class D IVD products including self-testing devices. Ensures regulatory compliance and market access across EU, UK, and Switzerland for IVD manufacturers and distributors.
Manufactured by
MedNet EC-REP GmbH
Münster, Germany
With many years of experience and a highly qualified team, MedNet EC-REP offers all services for the pan-European marketing authorization of your products: the European Authorized Representative (EC-REP), the UK Responsible Person (UK RP) and the Swiss Authorized Representative (CH-REP). We specialize in medical devices, in vitro diagnostics (IVD), personal protective equipment (PPE), clinical investigations and performance studies, and application for certificates of free sale (FSC).
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