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FTC4500

by Afikim Electric Vehicles

Ref AFISCOOTER C4Model AFISCOOTER C

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290018945AFISCOOTERC7D Basic UDI-DI 07290018945407UDI-DIDate17 May 2026RegisteredStatusActive

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  • Withdrawn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
Afiscooter C
Model / Reference
AFISCOOTER C, AFISCOOTER C4
Primary DI / UDI-DI
07290018945407
Basic UDI-DI
7290018945AFISCOOTERC7D
EMDN Code
Y122124 Electric scooters
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
IL-MF-000018381
Authorised representative
Arazy Group GmbH DE-AR-000007685

Other devices from Afikim Electric Vehicles (S.A.E. AFIKIM)

See all devices from Afikim Electric Vehicles (S.A.E. AFIKIM) →

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