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Tige fémorale X-PERT à cimenter

by Evolutis 17 variants

Ref H41 1701003Model Cemented Femoral Stems

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701271006148 Basic UDI-DI 03701271006148UDI-DIDate1 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

France
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • France

Specification

EUDAMED

Device Name
X-Pert
Model / Reference
Cemented Femoral Stems, H41 1701003
Primary DI / UDI-DI
03701271006148
Basic UDI-DI
B-03701271006148
EMDN Code
P090804010101 Cemented femoral stems for primary implant, with fixed neck, straight
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000492

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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