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Medial Rotation Knee

by MatOrtho Limited United Kingdom EUDAMED

Ref 156-712Model Medial Rotation Knee

EMDN P090903020301

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05055455504110 Basic UDI-DIDate13 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Medial Rotation Knee All Poly Tibia
Model / Reference
Medial Rotation Knee, 156-712
Primary DI / UDI-DI
05055455504110
Basic UDI-DI
B-05055455504110
EMDN Code
P090903020301 Bicompartmental primary implant tibial components, monoblock made of polyethylene
Device Class
Class III
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000007614
Authorised representative
MatOrtho Ireland Limited IE-AR-000006856

Other devices from MatOrtho Limited

See all devices from MatOrtho Limited →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 6e1da5e4-b05b-42d4-a225-829fd4e1f26b 61 fields · synced 25 Oct 2026