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Knee Walker

by shenzhenshi shenkehengjian yiliaokeji youxian gongsi 20 variants

Ref KW01-DModel KW01-A、KW01-B、KW01-C、KW01-D、KW01-E、KW01-F、KW01-G、KW01-H、KW01-I、KW01-J、KW01-K、KW01-L、KW01-M、KW01-N、KW01-P, 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 Number698053708KW001GW Basic UDI-DI 06980537086033UDI-DIDate25 Sep 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  • Withdrawn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
Knee Walker
Model / Reference
KW01-A、KW01-B、KW01-C、KW01-D、KW01-E、KW01-F、KW01-G、KW01-H、KW01-I、KW01-J、KW01-K、KW01-L、KW01-M、KW01-N、KW01-P, etc., KW01-D
Primary DI / UDI-DI
06980537086033
Basic UDI-DI
698053708KW001GW
EMDN Code
Y1299 Personal mobility devices - other
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000058886
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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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