EUDAMED checker / For consultants and authorised representatives

Device WatchMedTech & pharmaBeta

Watch every client SRN in EUDAMED.

Legacy devices must be registered in EUDAMED by 28 November 2026, and checking each client by hand in EUDAMED takes hours a week. Add your clients from a CSV and get one weekly email with what changed.

For: Regulatory consultants, EU authorised representatives and importers that follow many medical-device manufacturers.

Registration deadline for devices already on the market: 28 November 2026 (34 days left)

Look up any manufacturer first in the free EUDAMED checker: SRN, devices and certificates on the same data the digest uses.

What you get

  • Follow manufacturers by SRN, from a CSV or the API
  • One weekly digest: first device registrations, new UDI-DIs, certificate changes
  • The manufacturers with nothing registered yet, and the deadline countdown
  • EU and US FDA records joined per manufacturer

What the weekly digest shows

  • Deadline countdown to 28 November 2026 and how many of your manufacturers have devices registered, none yet, or a certificate expiring within 90 days.
  • This week: first device registrations, new UDI-DIs, and certificates issued, withdrawn or suspended, expired or expiring (with notified body and number).
  • Still to do: the manufacturers with no device in EUDAMED yet, and any followed SRN that EUDAMED does not list (a typo or a withdrawn actor).
  • Every line links to the manufacturer in the free EUDAMED checker.

Add your clients

Any CSV or text export of your client list works: every SRN in any column is followed, the other columns are ignored and never stored. In the API (self-serve key, not metered):

curl -X POST https://api.arcadiumdata.io/v1/watch/devices/bulk \
  -H "Authorization: Bearer $ARCADIUM_KEY" -H "content-type: application/json" \
  -d '{"csv": "client,srn\nAcme,DE-MF-000006413\nBeta,FR-MF-000012345"}'

The answer lists what was added, already followed, over your tier limit, and the lines without an SRN. Agents use the same route; the plans and limits are in GET /v1/plans (devicePortfolio). What has to be registered by when: EUDAMED deadline guide.

Source: EUDAMED, the European database on medical devices (European Commission), public data reused under Commission Decision 2011/833/EU (© European Union). Legal entities only. A registration, or its absence, is not proof of conformity or of non-compliance. Independent of the European Commission.

Pricing

Free

€0

  • 10 manufacturers
  • alert on a day with a change

Portfolio 50

€79 / month

  • 50 manufacturers (SRNs)
  • weekly digest, CSV bulk add

or €790 a year

Portfolio 250

€199 / month

  • 250 manufacturers (SRNs)
  • weekly digest, CSV bulk add

or €1,990 a year

Portfolio Unlimited

€399 / month

  • Unlimited (fair use 5,000)
  • weekly digest, CSV bulk add

or €3,990 a year

EUR, VAT exclusive. Yearly = two months free. Billed by invoice while self-serve checkout opens; a larger book or a feed into your own tools is the medical-device data licence.

Questions

Who is the portfolio for?

EU authorised representatives, importers and regulatory consultancies that follow the EUDAMED registrations of several manufacturers. Up to 10 manufacturers are free with the daily alert; a portfolio follows 50, 250 or your whole client book with one weekly digest.

What does the weekly digest contain?

One email every Monday for all the SRNs you follow: the days left to the 28 November 2026 registration deadline, which manufacturers registered their first device that week, new UDI-DIs, certificates issued, withdrawn, expired or expiring, the manufacturers with no device registered yet, and any SRN that EUDAMED does not list. Every line links to the record in the free EUDAMED checker.

How do I add my clients?

Upload a CSV or paste a list: every SRN like DE-MF-000006413 in any column is followed, other columns (client names, notes) are ignored and never stored. By API: POST /v1/watch/devices/bulk. SRNs already followed are skipped.

How is it billed?

Monthly or yearly (two months free), EUR, VAT exclusive, by invoice while self-serve checkout is being opened. Write to us with the tier you need; the account is switched on the day the order is confirmed.

Where does the data come from?

From the public EUDAMED database of the European Commission, read anonymously and refreshed daily. Legal entities only: names that read as a person and all contact details are left out. Arcadium Data is independent of the European Commission.

Sources

  • EUDAMED (European Commission)
  • US FDA establishment registrations (openFDA)

Guides: Eudamed deadline what manufacturers must register

Official public sources, read without logging in. Companies only, no personal data.