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ADM, a.s.

Active in EUDAMED

Czechiafrom SRN EUDAMED FDA SRN CZ-MF-000032589 FEI 3005347791

ADM, a.s. is a medical device manufacturer based in Czechia, with 64 devices listed in EUDAMED and FDA GUDID (EU Class IIa and I; FDA Class II) as of 12 Nov 2026.

Devices
64
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • EUDAMED 63
  • FDA GUDID 20

A device listed in two registries counts in both.

Device classes
  • EU Class IIa 49
  • EU Class I 8
  • FDA Class II 7
Top EMDN categories
Identifiers
  • EUDAMED SRN CZ-MF-000032589
  • FDA FEI 3005347791
  • DUNS 360589469

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

Catalogue64

Newest first, rows 1-50 of 64

Search and filter all 64 devices
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Rows 1-50 of 64

Showing 1-50 of 64

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
CZ-MF-000032589
FDA FEI number
3005347791
DUNS number
360589469
EU VAT number
CZ60742887
EUDAMED status
Active
EUDAMED registered name
ADM, a.s.
Registered address
2965/2, U Vodárny, 61600, Brno, Czechia
Website
adm.dental
PRRC contact
Zbynek Sedivy(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 30 Jul 2030

EUDAMED certificates (1)

INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390 1023 1 certificate

  • 25 0302 QR/NB Active

    Quality management system EU MDR

    Issued
    31 Jul 2025
    Expires
    30 Jul 2030

Frequently asked questions

How many devices does ADM, a.s. have in the registry?

The registry currently lists 64 devices for ADM, a.s.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ADM, a.s.'s devices?

Among its 50 most recently registered devices, ADM, a.s. has devices listed in EUDAMED (49 devices) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do ADM, a.s.'s devices fall under?

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

What EUDAMED certificates are recorded for ADM, a.s.?

EUDAMED lists 1 certificate for ADM, a.s. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 31 Jul 2025.

What are the newest devices from ADM, a.s. in the registry?

The most recently registered devices listed for ADM, a.s. include Fibrafill® FLOW Sample F-105, Fibrafill® FLOW F-005, Fibrafill® CUBE S F-001 and Fibrafill® CUBE S Sample F-101.

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