Authorized Representative services for Class I to Class III medical devices under MDR 2017/745, providing comprehensive EU regulatory compliance and market access.
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).
✦ Product-Specific Coverage
Based on AI-matched alternatives related to this product across Suplivia's medical sourcing network.
Generated for this product
AI-matched supplier coverage based on related product alternatives.
Prolinx GmbH
Germany · 2 relevant products
Metecon GmbH
Germany · 3 relevant products
MDSS USA LLC
United States · 5 relevant products
62 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →14 more sourcing countries available
Get free access to all sourcing countries identified for this product.
See all countries →See the full supplier coverage for this product
Get free access to all relevant manufacturers, sourcing countries, and product alternatives.
✓ Free for medical industry professionals.
from other manufacturers
from other manufacturers
3 of 104 closest product alternatives
Prolinx GmbH · Germany
EU regulatory compliance and market access services for medical device manufacturers, including authorized representative designation, MDR/IVDR registration, and CE marking documentation to facilitate entry into European markets.
Metecon GmbH · Germany
Regulatory representation services for medical devices and IVDs under MDR, IVDR, and related frameworks. EC-REP, CH-REP, and PRRC designation support enables market access and compliance across EU and international jurisdictions. Expert guidance on regulatory strategy, documentation, and post-market obligations.
MDSS USA LLC · United States
Regulatory representation and compliance service enabling non-EU medical device manufacturers to meet EU MDR, UK, Swiss, U.S., and Australian market requirements. Services include EU Authorized Representative designation, UK Responsible Person appointment, and clinical investigation sponsorship support across multiple jurisdictions.
101 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products