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Multigen Plus - H Tibial Augment #4 - H.7 Mm

by LIMACORPORATE S.p.A. EUDAMED

Active European Union

Ref 6621.15.407Model MULTIGEN PLUS, 80333903K024E7

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-08033390045278 Basic UDI-DIDate29 May 2026RegisteredStatusActive
European UnionCE/MDD NumberB-08033390045278 Basic UDI-DIDate29 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Certificates

1 certificate · EUDAMED

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

    Technical documentation EU MDR

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

Specification

EUDAMED

Trade Name
Multigen Plus - H Tibial Augment #4 - H.7 Mm
Multigen Plus Knee - TI6AL4V H Tibial Augment #4 - H=7MM
Model / Reference
MULTIGEN PLUS, 6621.15.407, 80333903K024E7
Primary DI / UDI-DI
08033390045278
Basic UDI-DI
B-08033390045278, 80333903K024E7
EMDN Code
P09098001 Knee prostheses augments
Device Class
Class III
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

Other properties (11)

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