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Manual Wheelchair

by Tianjin Taikang Sunshine Technology Co., Ltd 8 variants

Ref SYⅣ100-20A3

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 Number697080231006252 Basic UDI-DI 06970802310062UDI-DIDate12 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  • Withdrawn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
Manual Wheelchair
Model / Reference
SYⅣ100-20A3
Primary DI / UDI-DI
06970802310062
Basic UDI-DI
697080231006252
EMDN Code
Y122103 Push wheelchairs
Device Class
Class I
EU market of registration
Estonia

Manufacturer details

EUDAMED SRN
CN-MF-000008196
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Tianjin Taikang Sunshine Technology Co., Ltd

See all devices from Tianjin Taikang Sunshine Technology Co., Ltd →

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