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Dentapreg® SFU Sample

by ADM, a.s.

Ref D-051

Dentapreg® SFU Sample (D-051) is a Class IIa device made by ADM, a.s., registered in EUDAMED on 29 Aug 2025 (Basic UDI-DI 85956527SFU9Z), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number85956527SFU9Z Basic UDI-DI 08595652700108UDI-DIDate29 Aug 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Dentapreg® SFU
Model / reference
D-051
Primary DI / UDI-DI
08595652700108
Basic UDI-DI
85956527SFU9Z
EMDN code
Q010199 Conservative dentistry and endodontics devices - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000032589

Similar devices in this category

Other devices filed under CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER.

Other devices from ADM, a.s.

See all devices from ADM, a.s. →

Properties

Other properties (14, all answered No)