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Medial Rotation Knee

by MatOrtho Limited 60 variants

Ref 156-704Model 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-05055455504059 Basic UDI-DI 05055455504059UDI-DIDate13 May 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  • Withdrawn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 All Poly Tibia
Model / Reference
Medial Rotation Knee, 156-704
Primary DI / UDI-DI
05055455504059
Basic UDI-DI
B-05055455504059
EMDN Code
P090903020301 Bicompartmental primary implant tibial components, monoblock made of polyethylene
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

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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