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SENSODYNE Rapide Action Blancheur

by Haleon Medical Devices

Ref A1K0000000UM006

Active European Union

CE MDR

Valid until

15 Oct 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

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/MDR Number50596230DP000000000N909P Basic UDI-DI 05054563236623UDI-DIDate18 May 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • GB25/00000188 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    15 Oct 2025
    Expires
    15 Oct 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Stannous Fluoride 0.454% w/w Occluding Dentifrice
Model / Reference
A1K0000000UM006
Primary DI / UDI-DI
05054563236623
Basic UDI-DI
50596230DP000000000N909P
EMDN Code
Q0199 Odontology devices - other
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
IE-MF-000002458

Other devices from Haleon Medical Devices

See all devices from Haleon Medical Devices →

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