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Curasept Afte Rapid DNA Gel _EU Version

by Curasept S.p.A EUDAMED

Active European Union

Ref CS-04109Model CURASEPT AFTE RAPID DNA GEL 10 ML_EU VERSION

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08056746074067 Basic UDI-DIDate27 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
CURASEPT AFTE RAPID DNA GEL 10 ML_EU VERSION, CS-04109
Primary DI / UDI-DI
08056746074067
Basic UDI-DI
B-08056746074067
EMDN Code
Q019007 Buccal topical treatment preparations not included in other classes
Device Class
Class I
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