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Wingman

by Reflow Medical, Inc. EUDAMED

Active European Union

Ref WGM14150CEModel WGM, WMC, SPX, SPN, SLP

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number856492005SupportCathKP Basic UDI-DIDate20 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR 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

Model / Reference
WGM, WMC, SPX, SPN, SLP, WGM14150CE
Primary DI / UDI-DI
00856492005050
Basic UDI-DI
856492005SupportCathKP
EMDN Code
C0104020209 Peripheral vascular system total chronic occlusion devices
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
US-MF-000017521
Authorised representative
MediMark Europe Sarl. FR-AR-000000182

Other devices from Reflow Medical, Inc.

See all devices from Reflow Medical, Inc. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • 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