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Firefly 2.5

by Daedalus Wings Inc 2 variants

Ref 200-FGModel Firefly Fully Electric Wheelchair Attachment

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 Number0854126003fireflyQN Basic UDI-DI 00854126003243UDI-DIDate17 Feb 2023RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Firefly Fully Electric Wheelchair Attachment, 200-FG
Primary DI / UDI-DI
00854126003243
Basic UDI-DI
0854126003fireflyQN
Direct Marketing DI
00854126003243
EMDN Code
Y122410 Electric propulsion unit
Device Class
Class I
EU market of registration
Northern Ireland

Manufacturer details

EUDAMED SRN
US-MF-000032055
Authorised representative
Eurolink Europe Compliance Limited IE-AR-000002852

Other devices from Daedalus Wings Inc

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