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Crutch

by Xiamen KaiSheng Medical Instrument Co., Ltd 3 variants

Ref KS-YYG-001~0050Model KS-ZG-001~0050； KS-YG-001~0050；KS-YYG-001~0050

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number698047119CRUTNN Basic UDI-DI 06980471190032UDI-DIDate25 Aug 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  • Withdrawn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

Model / Reference
KS-ZG-001~0050； KS-YG-001~0050；KS-YYG-001~0050, KS-YYG-001~0050
Primary DI / UDI-DI
06980471190032
Basic UDI-DI
698047119CRUTNN
EMDN Code
Y12030601 Elbow crutches
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000041944
Authorised representative
Sungo Cert GmbH DE-AR-000010869

Other devices from Xiamen KaiSheng Medical Instrument Co., Ltd

See all devices from Xiamen KaiSheng Medical Instrument 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