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Incedo Foot Sensor Trial Kit

by Nordic-NeuroSTIM Denmark EUDAMED

Ref Foot Sensor Trial KitModel Incedo EMDN Z12062799

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5745000889_incedoYQ Basic UDI-DIDate6 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Incedo
Model / Reference
Incedo, Foot Sensor Trial Kit
Primary DI / UDI-DI
05745000889136
Basic UDI-DI
5745000889_incedoYQ
EMDN Code
Z12062799 Functional electrical stimulation systems - other
Device Class
Class IIa
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000001363

Other devices from Nordic-NeuroSTIM

See all devices from Nordic-NeuroSTIM →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 8e8cd4ee-7c03-4e8d-8669-3354bc6aba5d 61 fields · synced 23 Oct 2026