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Manyflow D 2 Vial

by Medex France EUDAMED

Ref FSDMU241, FSDMU240

EMDN A030499

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number37005504M0002YV Basic UDI-DIDate31 Jul 2025RegisteredStatusActive
European UnionCE/MDR Number37005504M0002YV Basic UDI-DIDate31 Jul 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDD, CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
ManyFlow/ Monoflow
Model / Reference
FSDMU241, FSDMU240
Primary DI / UDI-DI
13700550401039, 13700550400353
Basic UDI-DI
37005504M0002YV, B-13700550400353
EMDN Code
A030499 Administration kits - other
Device Class
Class IIa
Market of Registration
France
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000000414

Other devices from Medex

See all devices from Medex →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Animal Tissues
  • Administering Medicine
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (2)

  • EUDAMED 0d0dab81-772d-45ff-9ffc-ad6dd258837c 61 fields · synced 22 Oct 2026
  • EUDAMED 13700550400353|B-13700550400353 61 fields · synced 17 May 2026