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.
Manufactured by
MDSS USA LLC
Chicago, IL, United States
With over 30 years of experience, MDSS is a leading Authorized Representative and Regulatory Consulting organization, headquartered in Germany with offices in the United States, the United Kingdom, Switzerland, and Australia. Our services include: European Authorized Representative (EC REP) UK Responsible Person (UKRP) Swiss Authorized Representative (CH-REP) U.S. Agent Australian Sponsor Other services (e.g. Free Sales Certificates, GDPR, GPSR, Representative for Clinical Investigations, Vigilance, …) In addition to providing In-Country Representation services — helping streamline global market access through a single, reliable partner, so you can focus on your core business and innovation — we offer regulatory strategy consulting for medical devices and IVDs, support with pre-submissions and marketing authorization applications to the FDA , and assistance with EU MDR and EU IVDR compliance. Why MDSS? 30+ years of regulatory expertise Same trusted address for 20+ years Personalized support and tailored approach that sets MDSS apart from other regulatory service providers Collaborative network of offices spanning from the USA to Australia – single verification that grants access to three key markets: the EU, the UK, and Switzerland Independent services that protect your intellectual property Full control of your technical product files—no need to share with local importers or distributors MDSS is a member of the European Association of Authorized Representatives ( EAAR ), the UK Responsible Person Association ( UKRPA ), Swiss Medtech and the Medical Technology Association of Australia ( MTAA ).
✦ 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.
MedNet EC-REP GmbH
Germany · 15 relevant products
Obelis Group S.A.
Belgium · 3 relevant products
Metecon GmbH
Germany · 2 relevant products
60 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →13 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 113 closest product alternatives
MedNet EC-REP GmbH · Germany
European Authorized Representative (EU-REP) service providing regulatory compliance and market access support for medical devices, IVDs, cosmetics, and PPE across EU, UK, and Switzerland. Enables manufacturers to meet MDR 2017/745, IVDR 2017/746, and GPSR requirements for all device classes.
Obelis Group S.A. · Belgium
EU Authorised Representative service enabling medical device manufacturers and importers to demonstrate regulatory compliance with EU MDR/IVDR requirements. Provides expert guidance on EU, UK, US, and Swiss regulatory pathways for medical devices, in vitro diagnostics, and cosmetic products. Facilitates market access and post-market surveillance documentation.
MedNet EC-REP GmbH · Germany
European Authorized Representative service for medical devices, IVDs, cosmetics, and PPE across EU, UK, and Switzerland. Provides regulatory compliance, market access support, and notified body representation for Class I-III devices under MDR 2017/745 and IVDR 2017/746.
110 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products