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Myerson GanyMed

by The Myerson Company Limited 351 variants

Ref T92B1L0028

Active European Union

CE MDR

Valid until

16 Oct 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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 Number08423261TeethXK Basic UDI-DI 00842326184824UDI-DIDate19 Nov 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Preformed Artificial Teeth
Model / Reference
T92B1L0028
Primary DI / UDI-DI
00842326184824
Basic UDI-DI
08423261TeethXK
EMDN Code
P01020101 Dental implants
Device Class
Class IIa
EU 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

  • 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