Skip to content

BUCOMED CREMA FIJADORA 70g

by bonyf AG EUDAMED

Active European Union

Ref 223880.0

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7611645SU0300QV Basic UDI-DIDate6 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 50537-60-00-03 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0124
    Issued
    30 Jul 2026
    Expires
    18 Apr 2027
    Reason
    Other

Specification

EUDAMED

Device Name
Denture Adhesive Cream Superior
Model / Reference
223880.0
Primary DI / UDI-DI
08435232368833
Basic UDI-DI
7611645SU0300QV
EMDN Code
Q010280 Prosthetic dentistry devices - accessories
Device Class
Class IIa
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
LI-MF-000000739

Other devices from bonyf AG

See all devices from bonyf AG →

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