Skip to content

Medial Rotation Knee

by MatOrtho Limited EUDAMED

Active European Union

Ref 156-749Model Medial Rotation Knee

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05055455504417 Basic UDI-DIDate17 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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
Medial Rotation Knee All Poly Tibia
Model / Reference
Medial Rotation Knee, 156-749
Primary DI / UDI-DI
05055455504417
Basic UDI-DI
B-05055455504417
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

  • 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