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CURASEPT ADS DNA 212 200ml _ BUCOMED

by Curasept S.p.A

Ref CS-02245Model CURASEPT ADS DNA 212 200ml _ BUCOMED

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08056746073824 Basic UDI-DI 08056746073824UDI-DIDate9 Oct 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  • Withdrawn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

Model / Reference
CURASEPT ADS DNA 212 200ml _ BUCOMED, CS-02245
Primary DI / UDI-DI
08056746073824
Basic UDI-DI
B-08056746073824
EMDN Code
Q019007 Buccal topical treatment preparations not included in other classes
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000009299

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Properties

  • Animal Tissues
  • Incorporates Medicinal Product

Other properties (9)

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