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Subiton CIFO

by Laboratorios SL S.A. EUDAMED

Active European Union

Ref 885000Model Balón 10mm

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07798034468004 Basic UDI-DIDate27 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  • Withdrawn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
Sistema estéril de cifoplastía por balón – Componentes del set
Model / Reference
Balón 10mm, 885000
Primary DI / UDI-DI
07798034468004
Basic UDI-DI
B-07798034468004
EMDN Code
A019011 Intraosseous infusion and vertebroplasty infusion needles and kits
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

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: 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