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E-Walk, blybatteri, utan m-sats

by Decon Wheel AB EUDAMED

Withdrawn No longer placed on the EU market

Ref MCG4050

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number735001014MCGB3 Basic UDI-DIDate19 Oct 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
E-Walk
Model / Reference
MCG4050
Primary DI / UDI-DI
07350010140481
Basic UDI-DI
735001014MCGB3
EMDN Code
Y122410 Electric propulsion unit
Device Class
Class I

Manufacturer details

EUDAMED SRN
SE-MF-000046289

Other devices from Decon Wheel AB

See all devices from Decon Wheel AB →

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