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Manual Wheelchair

by Tianjin Linkang Medical Apparatus Co., Ltd.

Ref LK-801AModel Lk-801A Lk-801B Lk-801C LK-801C2 LK-801C3 LK-801C-DB LK-801-DE LK-801-SB LK-801C-SE LK-801S LK-802D LK807 LK808 LK809 etc

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 Number697672315LKMW01SP Basic UDI-DI 06976723150008UDI-DIDate29 Aug 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  • Withdrawn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

Device Name
Manual Wheelchair
Model / Reference
Lk-801A Lk-801B Lk-801C LK-801C2 LK-801C3 LK-801C-DB LK-801-DE LK-801-SB LK-801C-SE LK-801S LK-802D LK807 LK808 LK809 etc, LK-801A
Primary DI / UDI-DI
06976723150008
Basic UDI-DI
697672315LKMW01SP
EMDN Code
Y122103 Push wheelchairs
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000037261
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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