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Dentapreg® PFU Single

by ADM, a.s.

Ref D-523

Dentapreg® PFU Single (D-523) is a Class IIa device made by ADM, a.s., registered in EUDAMED on 28 Aug 2025 (Basic UDI-DI 85956527PFU9J), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number85956527PFU9J Basic UDI-DI 08595652700405UDI-DIDate28 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  • Withdrawn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® PFU
Model / reference
D-523
Primary DI / UDI-DI
08595652700405
Basic UDI-DI
85956527PFU9J
EMDN code
Q010299 Prosthetic dentistry 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 PROSTHETIC DENTISTRY DEVICES - OTHER.

Other devices from ADM, a.s.

See all devices from ADM, a.s. →

Properties

  • Implantable
Other properties (13, all answered No)