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Power Wheelchair

by Foshan Duson Medical Technology Co., Ltd.

Ref DS110, DS959LQModel DS110,DS110A,DS111,DS112,DS113,DS114,DS115,DS116,DS117,DS118,DS119,DS120,DS121,DS122,DS123,DS124,DS125,DS126,DS127,DS128,DS129,DS123GC, DS959LQ,DS950LBOPQ,DS959LQ,DS952LCQ,DS953LB,DS903LAJPQF9,DS957LQ,DS908LJ,DS863LAJPF4,DS903LQ,DS874LJF5,DS983L,DS907LABH,DS809L,DS874LAH,DS864LAJ,DS870LAJ,DS869LJ,DS863LABJ,DS863LAJ,DS872LAJP,DS864L,DS868L,DS871LBJ,DS976LABJF2-43

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 linked in EUDAMED

A group certificate may exist

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 Number697792826PW01VV Basic UDI-DI Date16 Oct 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Power Wheelchair
Wheel Chair
Model / Reference
DS110, DS110A, DS111, DS112, DS113, DS114, DS115, DS116, DS117, DS118, DS119, DS120, DS121, DS122, DS123, DS124, DS125, DS126, DS127, DS128, DS129, DS123GC, DS959LQ, DS950LBOPQ, DS952LCQ, DS953LB, DS903LAJPQF9, DS957LQ, DS908LJ, DS863LAJPF4, DS903LQ, DS874LJF5, DS983L, DS907LABH, DS809L, DS874LAH, DS864LAJ, DS870LAJ, DS869LJ, DS863LABJ, DS863LAJ, DS872LAJP, DS864L, DS868L, DS871LBJ, DS976LABJF2-43
Primary DI / UDI-DI
06977928261186, 06977928260028
Basic UDI-DI
697792826PW01VV, 697792826MW01V8
EMDN Code
Y122127, Y122103
Device Class
Class I
EU market of registration
Austria
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000044392
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Foshan Duson Medical Technology Co., Ltd.

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Properties

  • Reusable NoEUDAMEDYesEUDAMED

Other properties (12)

  • Sterile: No
  • Implantable: 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