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Medial Rotation Knee

by MatOrtho Limited EUDAMED

Active European Union

Ref 156-701Model Medial Rotation Knee

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05055455504028 Basic UDI-DIDate13 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Medial Rotation Knee All Poly Tibia
Model / Reference
Medial Rotation Knee, 156-701
Primary DI / UDI-DI
05055455504028
Basic UDI-DI
B-05055455504028
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

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Properties

  • Sterile
  • Implantable
  • Reprocessed

Other properties (8)

  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No