The clock is ticking for the European medical device industry.
On 28 May 2026, the mandatory use of the first EUDAMED modules officially begins, following the end of the six‑month transition period. From that date onwards, economic operators under MDR and IVDR must comply with the use of key EUDAMED modules, including:
- Actor Registration (SRN)
- UDI / Device Registration
- Notified Bodies & Certificates
- Market Surveillance
If your organization hasn’t fully prepared yet, now is the moment to act. Delaying could put compliance, certifications, and market access at risk.
Whether you are still setting up your registrations or already populating data, the right support can make the difference between last‑minute stress and a smooth transition.
At Starodub, we support organizations specifically with Actor Registration (SRN) and UDI / Device Registration, helping you approach EUDAMED confidently as the deadline approaches.
Get in touch — 28 May is closer than you think! Contact us at [email protected]
