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Espaciadores de prueba cadera Subiton

by Laboratorios SL S.A. EUDAMED

Active European Union

Ref 882005Model Cadera (Müller y Charnley)

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07798034467311 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

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.

Specification

EUDAMED

Device Name
Espaciador de prueba de cadera
Model / Reference
Cadera (Müller y Charnley), 882005
Primary DI / UDI-DI
07798034467311
Basic UDI-DI
B-07798034467311
EMDN Code
L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
AR-MF-000023153
Authorised representative
Synergie Ingénierie Médicale FR-AR-000001802

Other devices from Laboratorios SL S.A.

See all devices from Laboratorios SL S.A. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: 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