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Solax

by Guangdong Prestige Technology Co., Ltd. 10 variants

Ref S302421G BlueModel S302421G

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697099083S3024H8 Basic UDI-DI 06970990836009UDI-DIDate3 Jun 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  • Withdrawn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
Electric Scooter
Model / Reference
S302421G, S302421G Blue
Primary DI / UDI-DI
06970990836009
Basic UDI-DI
697099083S3024H8
EMDN Code
Y122124 Electric scooters
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000017186
Authorised representative
Share info GmbH DE-AR-000005132

Other devices from Guangdong Prestige Technology Company Limited

See all devices from Guangdong Prestige Technology Company Limited →

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