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Vástago Femoral Autobloqueante No Cementado Con Plasma De Titanio

by Surgival Co., S.A.U. 9 variants

Ref A1502012EModel VÁSTAGO FEMORAL AUTOBLOQUEANTE NO CEMENTADO CON PLASMA DE TITANIO

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08435225800890 Basic UDI-DI 08435225800890UDI-DIDate19 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  • Withdrawn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

Model / Reference
VÁSTAGO FEMORAL AUTOBLOQUEANTE NO CEMENTADO CON PLASMA DE TITANIO, A1502012E
Primary DI / UDI-DI
08435225800890
Basic UDI-DI
B-08435225800890
EMDN Code
P090804010201 Uncemented femoral stems for primary implant, with fixed neck, straight
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000028629

Other devices from Surgival Co., S.A.U.

See all devices from Surgival Co., S.A.U. →

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