Skip to content

Multigen Plus COCRMO+UHMWPE+TI6AL4V Hinged Knee H Tibial Liner+hinge #1 - H=12MM

by LIMACORPORATE S.p.A.

Ref 6660.50.112Model 80333903K022E3

Active European Union

CE MDR

Valid until

10 Sep 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ITALCERT SRL

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80333903K022E3 Basic UDI-DI 08033390044981UDI-DIDate10 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 053-00-02-MDR Active Supplemented

    Technical documentation EU MDR

    Certifier
    ITALCERT SRL 0426
    Issued
    14 Oct 2025
    Expires
    10 Sep 2029
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
80333903K022E3, 6660.50.112
Primary DI / UDI-DI
08033390044981
Basic UDI-DI
80333903K022E3
EMDN Code
P090905020201 Revision knee prostheses mobile bearing tibial inserts
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010690

Other devices from LIMACORPORATE S.p.A.

See all devices from LIMACORPORATE S.p.A. →

Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

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