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Tibiaplatte GEMINUS-V distal, ventral, polyaxial winkelstabil, rechts, 4 Loch, Titan

by INTERCUS GmbH EUDAMED 2 variants

Active European Union

Ref 750.521444Model Tibiaplatte "GEMINUS-V" distal, ventral, polyaxial winkelstabil, rechts, 4 Loch, Titan

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number4052024-ws-Platte+TB Basic UDI-DIDate14 Oct 2026RegisteredStatusActive
European UnionCE/MDR Number4052024-ws-Platte+TB Basic UDI-DIDate14 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
winkelstabile Platten
Model / Reference
750.521444, Tibiaplatte "GEMINUS-V" distal, ventral, polyaxial winkelstabil, rechts, 4 Loch, Titan
Primary DI / UDI-DI
04052024047673
Basic UDI-DI
4052024-ws-Platte+TB, B-04052024047673
EMDN Code
P09120502 Osteosynthesis neutralisation and support plates
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005084

Other devices from INTERCUS GmbH

See all devices from INTERCUS GmbH →

Properties

  • Implantable
  • Sutures

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