Your Trusted Partner for Global Regulatory Compliance

Your In-Country Representative For Medical Device Compliance in the EU, UK, CH & US

We support manufacturers of Medical Devices and IVDs with one-stop shop solutions for compliance 

IVDs need a Notified Body appointed by 26 May 2026

Do not risk non-compliance!

Why Obelis? 

Experience

Founded in 1988, we are among Europe’s largest centres for advisory and representative services.

ISO Certification

We are certified by ISO 9001:2015 and ISO 13485:2016.

Commitment to Compliance

We have helped over 3,000 manufacturers from over 60 countries address their regulatory challenges.

Proximity to EU Institutions

We are members of professional associations and more than 10 European Commission working groups.

International Network

Obelis International Offices (OIO) comprise independent partners providing solutions in other global markets.

Our Team

Our team consists of lawyers, chemists, pharmacists, and other experts. 

Get our free supporting tools

Download it now:

Obelis Group

Boulevard Brand Whitlock 30, 

Brussels, 1200, Belgium

Tel: +32 (0)2 732 59 54

sales@obelis.net

© Obelis Group 2026

Information platforms

Mdlaw.eu

Coslaw.eu

Prodlaw.eu

EU, UK, CH, US

About Us

  • Authorised Representation (EC REP)/ Responsible Person (UK RP)
  • EUDAMED device and actor registration
  • Device registrations to the EU & UK authorities (MHRA)
  • MedDO/ IvDO & MDR/ IVDR technical documentation review
  • Assist with CE & UKCA marking 
  • Vigilance and incidence reporting  
  • MDlaw.eu news, alerts, templates and guidelines
  • Compliance trainings

Client Success stories

The EUDAMED verification and mandate update were completed successfully, allowing us to maintain our devices on the EU market without any regulatory issues or interruptions. The process was efficient and well managed.

We successfully maintained our EU market access

Biobeat Technologies Ltd.

With Obelis’ support, our device was successfully registered on the MHRA portal. We’re now ready to place our product on the UK market with full confidence. Without their guidance, the process would have been far more stressful and prone to delays.

We're now ready to place our product on the UK market with confidence

Koravie Limited

Obelis brought the clarity we needed. Their in-depth regulatory knowledge and ability to act swiftly made a real difference. They weren’t just service providers, they were collaborators.

Obelsi brought the clarity we needed when it mattered most

Medical Devices (Pvt) Ltd.

We register your products in the EU, UK and Switzerland in 3 working days