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Uni Gal Hap Fem Comp Ri/Le S5

by groupe lépine

Ref GGU FH005

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+M483GGUFH0050 Basic UDI-DI +M483GGUFH0050UDI-DIDate22 Oct 2026RegisteredStatusActive

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  • Withdrawn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
GALICA UNI Ti/HA FEMUR
Model / Reference
GGU FH005
Primary DI / UDI-DI
+M483GGUFH0050
Basic UDI-DI
B-+M483GGUFH0050
EMDN Code
P0909040102 Unicompartmental knee prostheses femoral components (unicondylar), uncemented
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001182

Other devices from groupe lépine

See all devices from groupe lépine →

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