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Vxsy-10-1-Ch

by OPED GmbH EUDAMED

Withdrawn Not intended for the EU market

Ref VXSY-10-1-CHModel VXSY-10-1

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4046618Z120607VX8H Basic UDI-DIDate13 Apr 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
VADOplex
Model / Reference
VXSY-10-1, VXSY-10-1-CH
Primary DI / UDI-DI
04046618014462
Basic UDI-DI
4046618Z120607VX8H
EMDN Code
Z120607 Pneumatic compression equipment
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
DE-MF-000008286

Other devices from OPED GmbH

See all devices from OPED GmbH →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • 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