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blend-a-dent

by Procter & Gamble Technical Centres Limited EUDAMED

Active European Union

Ref 80812240

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8001090dentadhZF Basic UDI-DIDate24 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Denture Adhesive
Model / Reference
80812240
Primary DI / UDI-DI
08700216580823
Basic UDI-DI
8001090dentadhZF
Unit of Use DI
08700216191753
EMDN Code
Q010280 Prosthetic dentistry devices - accessories
Device Class
Class IIa
Market of Registration
Romania

Manufacturer details

EUDAMED SRN
GB-MF-000017862
Authorised representative
Procter & Gamble Service GmbH DE-AR-000016615

Other devices from Procter & Gamble Technical Centres Limited

See all devices from Procter & Gamble Technical Centres Limited →

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