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Vastago Femoral Revision Karey-C Cementado

by Surgival Co., S.A.U. 34 variants

Ref F0530919EModel VASTAGO FEMORAL REVISION KAREY-C CEMENTADO

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-08435226202877 Basic UDI-DI 08435226202877UDI-DIDate14 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

Spain
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • Spain

Specification

EUDAMED

Model / Reference
VASTAGO FEMORAL REVISION KAREY-C CEMENTADO, F0530919E
Primary DI / UDI-DI
08435226202877
Basic UDI-DI
B-08435226202877
EMDN Code
P090804030101 Revision cemented femoral stems, with fixed neck
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000028629

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

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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