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Curasept Biosmalto Dentifrcio Denti Sensibili

by Curasept S.p.A

Ref CS-02370Model CURASEPT BIOSMALTO DENTIFRICIO DENTI SENSIBILI 75ML

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08056746071561 Basic UDI-DI 08056746071561UDI-DIDate27 Aug 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Trade Name
Curasept Biosmalto Dentifrcio Denti Sensibili
Curasept Biosmalto Dentifricio Denti Sensibili
Model / Reference
CURASEPT BIOSMALTO DENTIFRICIO DENTI SENSIBILI 75ML, CS-02370
Primary DI / UDI-DI
08056746071561
Basic UDI-DI
B-08056746071561, 805674607BIODDS07XL
Direct Marketing DI
08056746071561
EMDN Code
Q019008, Q0199
Device Class
Class I
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000009299

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Properties

Other properties (13)

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