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Fisiograft

by Ghimas S.p.A. Italy EUDAMED

Ref Fisiograft

EMDN P900401

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FISIOGRAFT12CZ Basic UDI-DIDate21 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Fisiograft
Model / Reference
Fisiograft
Primary DI / UDI-DI
D-FISIOGRAFT12CZ
Basic UDI-DI
B-FISIOGRAFT12CZ
EMDN Code
P900401 Bone and tendon replacement devices
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000017070

Other devices from Ghimas S.p.A.

See all devices from Ghimas S.p.A. →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED fe98cc2d-1e53-491a-88f9-a422e68d446c 61 fields · synced 24 Oct 2026