EudaMed Check gives manufacturers, importers, procurement teams and compliance managers instant access to certified EUDAMED data — market intelligence, portfolio verification, competitor analysis and regulatory monitoring.
Manufacturer Export
Full UDI-DI dataset for your SRN. PDF + JSON ready for audit.
Market Intelligence
Scan entire EMDN categories — see every competitor device.
Tender Package
Certified letter + verifiable buyer code for procurement.
Portfolio Check
Verify your full device portfolio is correctly registered.
PRRC Monitor
Weekly compliance reports per MDR Article 83 obligations.
Hospital Procurement
Verify any supplier SRN instantly. No permissions needed.
MI Notifications
Automated alerts when competitor registrations change.
AR Mandate Check
Verify Authorised Representative mandates & representation certificates.
Eight distinct services built for every team that touches EUDAMED data.
Get a certified export of all your EUDAMED submissions — your full UDI-DI dataset, SRN status, certificate details and device data in PDF and machine-readable JSON. Perfect for internal audits, board reports and regulatory dossiers.
Scan entire EMDN product categories and see every registered medical device, manufacturer and notified body across the EU. Competitive analysis, market sizing and gap analysis — all from live EUDAMED data.
Win public tenders with a certified EudaMed Check tender letter. Each report includes a unique verifiable code that procurement teams can validate independently — proof that your device data is live and correct.
You are legally required under MDR Article 13 to verify that your supplier's UDI-DI is correctly registered. EudaMed Check validates your entire supplier list against live EUDAMED data and flags any discrepancies.
EudaMed Monitor delivers a weekly automated report of your EUDAMED registration status — covering all devices under your SRN, flagging any changes, and providing the MDR Article 83 post-market surveillance evidence trail.
Verify any medical device supplier's EUDAMED registration instantly. No supplier permission required. Check that the devices you are procuring are correctly registered and compliant — before contract award.
Receive automated Market Intelligence Notifications the moment competitor device registrations change in EUDAMED — new devices added, certificates updated, or registrations lapsed. Stay ahead without manual monitoring.
Verify that your Authorised Representative's mandate and Representation Certificate are correctly reflected in EUDAMED. Essential for MDR Article 11 compliance and Notified Body audit readiness.
No account. No waiting. Just certified EUDAMED data.
Visit eudamedcheck.com and choose from six report types — Manufacturer Export, Market Scan, Tender Package, Portfolio Check, PRRC Monitor or Hospital Procurement.
Enter your SRN, EMDN category, device list or supplier name. Our system queries live EUDAMED data directly from the European Commission's database.
Your certified PDF and JSON report is delivered instantly. Each report includes a verifiable code, EirMed certification, and a timestamp of the data pull.
EUDAMED contains registration data for every medical device sold in the EU. EudaMed Check unlocks that intelligence — scan any EMDN product category and get a complete picture of who is registered, what devices they have, and which notified bodies they use.
Market sizing
How many devices are registered in your EMDN category?
Competitor mapping
Which manufacturers are registered and what is their portfolio?
Notified body landscape
Which NBs are being used across your product category?
Registration timeline
When did competitors register? Who is newest to the market?
With EUDAMED becoming mandatory on 28 May 2026, every UDI-DI must be correctly registered. EudaMed Check verifies your complete portfolio against live EUDAMED data — flagging missing registrations, pending submissions, and data discrepancies before they become compliance issues.
Everything you need from EUDAMED data — available now at eudamedcheck.com
Complete UDI-DI dataset, certificate details and device data for one SRN. PDF + JSON. Ready for board reports, audits and regulatory dossiers.
All registered devices in an EMDN category across every manufacturer in the EU. Competitor analysis, market sizing, NB landscape.
Certified report with verifiable buyer code. Accepted by EU public procurement authorities as proof of EUDAMED registration.
Verify your entire supplier UDI-DI list against live EUDAMED — required under MDR Article 13. Flags missing and incorrect registrations.
Automated weekly PRRC compliance monitoring. Covers all devices under your SRN. MDR Article 83 post-market surveillance evidence trail.
Verify any supplier EUDAMED SRN instantly. No supplier permission required. Confirm compliance before contract award.
Automated alerts the moment competitor device registrations change in EUDAMED — new devices, updated certificates, lapsed registrations.
Verify that your Authorised Representative mandate and Representation Certificate are correctly reflected in EUDAMED. MDR Article 11 compliance.
Certified by EirMed — eudamedcheck.com
Visit eudamedcheck.com now — or contact EirMed to arrange a demonstration for your team.
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