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OlivaFix® Denture Adhesive cream

by bonyf AG

Ref 5.970.00.T.0.0.00

Expiring European Union

CE MDR

Valid until

18 Apr 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DEKRA Certification GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50537-60-00-03 Date30 Jul 2026IssuedStatusExpiring expires 18 Apr 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 50537-60-00-03 Expiring Supplemented Expires in 168 days

    Quality management system EU MDR

    Certifier
    DEKRA Certification GmbH 0124
    Issued
    30 Jul 2026
    Expires
    18 Apr 2027
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
OlivaFix® / OlivaFix® Fresh Denture Adhesive cream
Model / Reference
5.970.00.T.0.0.00
Primary DI / UDI-DI
07611645597003
Basic UDI-DI
7611645OL0400LB
EMDN Code
Q010280 Prosthetic dentistry devices - accessories
Device Class
Class IIa
EU market of registration
France

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