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VACOpedes

by OPED GmbH EUDAMED

Active European Union

Ref VEDE-01-4-S

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4046618Y0612VEBX Basic UDI-DIDate9 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenSwedenSwedenSwedenEstoniaIrelandNetherlandsFranceBelgiumLuxembourgCzech RepublicFranceFranceAustriaFranceFranceSlovenia
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

EU market availability

Available in 10 countries, as listed in EUDAMED:

  • Austria since 9 Sep 2025
  • Belgium since 15 Feb 2017
  • Czechia since 12 Jun 2015
  • Estonia since 6 Aug 2025
  • France since 11 Apr 2013
  • Ireland since 26 Mar 2013
  • Luxembourg since 18 Feb 2016
  • Netherlands since 26 Jul 2012
  • Slovenia since 23 Jan 2014
  • Sweden since 11 Mar 2016

Last checked 24 Oct 2026.

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
VACOpedes
Model / Reference
VEDE-01-4-S
Primary DI / UDI-DI
04046618087015
Basic UDI-DI
4046618Y0612VEBX
EMDN Code
Y061203 Orthoses, foot (including insoles and inserts)
Device Class
Class I
Market of Registration
Netherlands

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