Skip to content

Medial Rotation Knee

by MatOrtho Limited 60 variants

Ref 156-825Model Medial Rotation Knee

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-05055455504851 Basic UDI-DI 05055455504851UDI-DIDate21 Apr 2022RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Medial Rotation Knee Patella
Model / Reference
Medial Rotation Knee, 156-825
Primary DI / UDI-DI
05055455504851
Basic UDI-DI
B-05055455504851
EMDN Code
P0909070201 Patellar components, monoblock
Device Class
Class III
EU 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