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Denture Relining Cushion Stabilizer

by bonyf AG Liechtenstein EUDAMED

Ref 6.000.01.X.0.0.00 EMDN Q010503

Regulatory status

as of 26 Oct 2026

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

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  • Withdrawn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 · synced 24 Oct 2026

Model / Reference
6.000.01.X.0.0.00
Primary DI / UDI-DI
07611645000060
Basic UDI-DI
7611645RE0600KF
EMDN Code
Q010503 Impression material trays, single-use
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
LI-MF-000000739

Other devices from bonyf AG

See all devices from bonyf AG →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 869674da-cbf7-4399-9021-bede4e2b5f47 61 fields · synced 24 Oct 2026