Skip to content

Perfuseus à usage unique

by Societe de Fabrication des Articles Pharmaceutiques SO.F.A.P Ltd Tunisia EUDAMED

Ref PS2a23SLLAModel les variants ;Chambre de goutement,tubulure,embout

EMDN A03010103

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number61924931PERFUSEURW7 Basic UDI-DIDate21 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
perfuseur a usage unique
Model / Reference
les variants, Chambre de goutement, tubulure, embout, PS2a23SLLA
Primary DI / UDI-DI
06192493100887
Basic UDI-DI
61924931PERFUSEURW7
EMDN Code
A03010103 Infusion controllers with flow regulator
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
TN-MF-000023623
Authorised representative
Obelis s.a. BE-AR-000000106

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Administering Medicine
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 58b8326d-1e61-4b7d-8390-b279206da224 61 fields · synced 22 Oct 2026