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).
✦ 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.
MDSS USA LLC
United States · 5 relevant products
Metecon GmbH
Germany · 3 relevant products
Obelis Group S.A.
Belgium · 3 relevant products
40 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →12 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 72 closest product alternatives
MDSS USA LLC · United States
Regulatory consulting and in-country representation services for medical devices and IVDs across EU, UK, Switzerland, USA, and Australia. Enables non-domestic manufacturers to achieve market compliance and maintain regulatory standing in multiple jurisdictions through appointment as Authorized Representative or equivalent legal entity.
MDSS USA LLC · United States
UK Responsible Person (UKRP) representation service for medical devices and IVDs seeking market authorization in the United Kingdom. Ensures regulatory compliance with UK MDR requirements and facilitates in-country representation for non-UK established manufacturers.
MDSS USA LLC · United States
European Authorized Representative and regulatory compliance service for medical devices and IVDs. Provides in-country representation across EU, UK, Switzerland, USA, and Australia to ensure manufacturers meet MDR, IVDR, AI Act, and GDPR requirements.
69 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products