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Cabeza Femoral Endocefálica

by Surgival Co., S.A.U. 19 variants

Ref A1513252EModel CABEZA FEMORAL ENDOCEFÁLICA

Active European Union

CE MDR

Valid until

5 Feb 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number84352258IMP10500012T Basic UDI-DI 08435225802221UDI-DIDate23 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2026 DR 0091 Active

    Technical documentation EU MDR

    Certifier
    CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS 0318
    Issued
    9 Jun 2026
    Expires
    5 Feb 2029

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
CABEZA FEMORAL ENDOCEFÁLICA, A1513252E
Primary DI / UDI-DI
08435225802221
Basic UDI-DI
84352258IMP10500012T
EMDN Code
P090804050102 Metal femoral heads, partial hip replacement
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