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Clignsetfk

by bredent GmbH & Co. KG

Ref CLIGNSETFKModel system crea.lign paste gel

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EBRESystCreaPasteGel3V Basic UDI-DI +EBRECLIGNSETFK02UDI-DIDate16 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
system crea.lign paste gel, CLIGNSETFK
Primary DI / UDI-DI
+EBRECLIGNSETFK02
Basic UDI-DI
++EBRESystCreaPasteGel3V
EMDN Code
Q01010104, Q0102050199
Device Class
Class IIa
Medical Purpose
Dental restoration

Manufacturer details

EUDAMED SRN
DE-PR-000014120

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Properties

Other properties (1)

  • Sterile: No