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V-Wave™ Ventura® Interatrial Shunt

by V-Wave Ltd.

Ref VIS-01-5.0-14F

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-IL-MF-000030090XH Basic UDI-DI D-IL-MF-000030090XHUDI-DIDate11 Jan 2023RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
V‐Wave™ Ventura® Interatrial Shunt System
Model / Reference
VIS-01-5.0-14F
Primary DI / UDI-DI
D-IL-MF-000030090XH
Basic UDI-DI
B-IL-MF-000030090XH
EMDN Code
C019015, C99
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000030090
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from V-Wave Ltd.

Properties

  • Sterile
  • Implantable

Other properties (9)

  • 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