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Curasept Biosmalto Sens.imp. Act Mousse Trays V1

by Curasept S.p.A

Ref CS-02374Model CURASEPT BIOSMALTO SENS.IMP. ACT MOUSSE TRAYS V1

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08056746072407 Basic UDI-DI 08056746072407UDI-DIDate28 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Curasept Biosmalto Sensitive Teeth .imp. Act Mousse Trays
Model / Reference
CURASEPT BIOSMALTO SENS.IMP. ACT MOUSSE TRAYS V1, CS-02374
Primary DI / UDI-DI
08056746072407
Basic UDI-DI
B-08056746072407
EMDN Code
Q019008 Dentinal desensitisers
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
IT-MF-000009299

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Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No