Independent guidance · EU market access
Get registered in EUDAMED before 28 November — without drowning your team.
Know where you stand. Close the gaps. Connect with an independent EU specialist for the work ahead.
Free public-record check · Specialist referrals · No obligation
The right kind of expertise
EU Authorised RepresentativesRegulatory consultanciesUDI data specialistsA clearer starting point
Does your team need to act?
Three questions. An instant starting point. Your answers stay in this browser.
From uncertainty to a next step
You do not need to
untangle it alone.
- 01
Answer 3 questions
Use the checker above to see where your registration work may need attention.
- 02
Get a free registration check
We review your company’s public actor and device records and send a short findings note.
- 03
Connect with an EU specialist
Tell us what support you need. Your submission consent lets us share your details with one matched independent specialist.
Start with the essentials
Clear answers.
Primary sources.
Which deadline applies to your portfolio?
Understand mandatory use from 28 May 2026, the November transition, and certificate registration.
Do you have the right SRN?
Actor registration comes first. Prepare the identity, mandate, and access details you need.
How should your device records fit together?
A practical explanation of Basic UDI-DI, UDI-DI, and legacy identifiers.
Selling into the EU from the US?
Clarify the split between your team, your Authorised Representative, and your importer.
Your next step
Start with what the public record shows.
Request a free check, or tell us where you need support for an introduction to an independent specialist.
No obligation. No promise of a regulatory outcome.