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Anaftin Plus Spray

by Alliance Pharma Srl

Ref 604297/507393/529633/590846/662893/577108/587260/566054Model Aloclair Plus

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-04013054025161 Basic UDI-DI 04013054025161UDI-DIDate16 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  • Withdrawn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
Aloclair Plus, 604297/507393/529633/590846/662893/577108/587260/566054
Primary DI / UDI-DI
04013054025161
Basic UDI-DI
B-04013054025161
EMDN Code
Q019007 Buccal topical treatment preparations not included in other classes
Device Class
Class IIa
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
IT-MF-000030271

Other devices from Alliance Pharma Srl

See all devices from Alliance Pharma Srl →

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