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Myerson GanyMed

by The Myerson Company Limited United States EUDAMED

Ref T92B1U0F35 EMDN P01020101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08423261TeethXK Basic UDI-DIDate19 Nov 2025RegisteredStatusActive

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  • Withdrawn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 · synced 25 Oct 2026

Device Name
Preformed Artificial Teeth
Model / Reference
T92B1U0F35
Primary DI / UDI-DI
00842326185814
Basic UDI-DI
08423261TeethXK
EMDN Code
P01020101 Dental implants
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
TT-MF-000045141
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from The Myerson Company Limited

See all devices from The Myerson Company Limited →

Properties & raw data

Show properties, registry sources and raw records
  • Implantable
Other properties (12)
  • Sterile: 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 00842326185814|08423261TEETHXK 61 fields · synced 25 Oct 2026