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V-Wave Ventura® Delivery System

by V-Wave Ltd. EUDAMED

Active European Union

Ref VDS-02-0.0-14F85

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290017258027 Basic UDI-DIDate29 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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
V-Wave® Ventura® Delivery System
Model / Reference
VDS-02-0.0-14F85
Primary DI / UDI-DI
07290017258027
Basic UDI-DI
B-07290017258027
EMDN Code
C99 Cardiocirculatory devices - other
Device Class
Class III
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
  • Reprocessed

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No