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Wheeled Walker

by Unitrend Co., Ltd. 3 variants

Ref SP-100-LEOModel Wheeled Walker

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 Number471988232RWKC00018C Basic UDI-DI 04719882320705UDI-DIDate4 Apr 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  • Withdrawn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
Wheeled Walker
Model / Reference
Wheeled Walker, SP-100-LEO
Primary DI / UDI-DI
04719882320705
Basic UDI-DI
471988232RWKC00018C
Direct Marketing DI
04719882320705
EMDN Code
Y120606 Wheeled walker
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
TW-MF-000012250
Authorised representative
KOMAS Medical Technology GmbH DE-AR-000045617

Other devices from Unitrend Co., Ltd.

See all devices from Unitrend 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