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Serres Oy

Active in EUDAMED

Finlandfrom SRN EUDAMED FDA SRN FI-MF-000004504 FEI 3010300504

Serres Oy is a medical device manufacturer based in Finland, with 204 devices listed in EUDAMED and FDA GUDID (EU Class I; FDA Class II) as of 13 Nov 2026.

Devices
204
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • EUDAMED 198
  • FDA GUDID 73

A device listed in two registries counts in both.

Device classes
  • EU Class I 198
  • FDA Class II 6
Identifiers
  • EUDAMED SRN FI-MF-000004504
  • FDA FEI 3010300504
  • DUNS 401738638

At a glance

Counted by deviCERTS from registry records

EU certificates

2 of 2 in force.

See certificates

Market reach

European Union
EUDAMED actor, 2 certificates
United States
FDA FEI

Catalogue204

Newest first, rows 1-50 of 204

Search and filter all 204 devices
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Rows 1-50 of 204

Showing 1-50 of 204

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
FI-MF-000004504
FDA FEI number
3010300504
DUNS number
401738638
EU VAT number
FI05917213
EUDAMED status
Active
EUDAMED registered name
Serres Oy
Registered address
23, Keskustie, 61850, Kauhajoki as., Finland
Phone
+358 20 746 4400
PRRC contact
Katriina Kottelin(public in EUDAMED)

EUDAMED certificates2

2 certificates2 valid, 0 expiredMDR 2next expiry 27 Nov 2027

EUDAMED certificates (2)

SGS FIMKO OY 0598 2 certificates

  • FI22/00000016 Active Reissued

    Quality management system EU MDR

    Issued
    24 Oct 2025
    Expires
    24 Oct 2030
    Valid from
    25 Oct 2025
  • FI22/00000016 Active Amended

    Quality management system EU MDR

    Issued
    11 Mar 2024
    Expires
    27 Nov 2027
    Reason
    Other

Frequently asked questions

How many devices does Serres Oy have in the registry?

The registry currently lists 204 devices for Serres Oy. Devices recorded under merged duplicate company entries are counted once.

Which registries list Serres Oy's devices?

Among its 50 most recently registered devices, Serres Oy has devices listed in EUDAMED (44 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Serres Oy's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Serres Oy's devices are Class I and Class II. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Serres Oy?

EUDAMED lists 2 certificates for Serres Oy (quality management system) under MDR. The most recent was issued on 24 Oct 2025.

What are the newest devices from Serres Oy in the registry?

The most recently registered devices listed for Serres Oy include Vacuum tubing, silicone, Wall bracket, plastic, Serres Sylva bC 3000ml valve and Measuring cup.

Generated automatically from registry data and not verified by a human reviewer.