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Mobile Dream standard abdominale gachette gauche vert

by Lazelec

Ref Mobile Dream standard abdominale gachette gauche vertModel Mobile Dream

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376040090MOBILE-DREAM6R Basic UDI-DI 03760400901495UDI-DIDate29 Apr 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Mobile Dream
Model / Reference
Mobile Dream, Mobile Dream standard abdominale gachette gauche vert
Primary DI / UDI-DI
03760400901495
Basic UDI-DI
376040090MOBILE-DREAM6R
Direct Marketing DI
03760400901495
EMDN Code
Y122199 Wheelchairs - other
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000007150

Other devices from Lazelec

See all devices from Lazelec →

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