U.S. Agent representation service enabling non-U.S. medical device and IVD manufacturers to establish compliant market access in the United States. Provides regulatory expertise, documentation management, and liaison with FDA for devices requiring in-country representation.
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 ).
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Obelis Group S.A. · Belgium
U.S. Agent and Official Correspondent service for medical device manufacturers seeking FDA compliance and regulatory representation. Facilitates regulatory submissions, communications with FDA, and ensures adherence to U.S. medical device regulations for market authorization and post-market surveillance.
Maven Profcon Services LLP · India
Regulatory consulting services supporting medical device and IVD manufacturers through CE marking, US FDA 510(k) clearance, and UKCA certification. Services include technical documentation preparation, conformity assessment, clinical evaluation, risk management, and audit support to ensure compliance with EU MDR, EU IVDR, and UK regulatory requirements.
EUCEREP B.V. · Netherlands
Regulatory representation and compliance service enabling non-EU manufacturers to obtain EU Authorized Representative (EAR) and UK Responsible Person (UKRP) status for medical device market access. Supports CE marking, EUDAMED registration, technical documentation, and Quality Management System establishment to meet European and UK regulatory requirements.
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