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Rollator

by Zhongshan KDB Health Solutions Co. Ltd. EUDAMED

Active European Union

Ref KDBWG917C-AModel KDBWG917B-A,KDBWG917B-B,KDBWG917C-A,KDBWG917C-B,KDBWG917D,KDBWG917E,KDBWG917F,KDBWG917G,KDBWG917H,KDBWG917I,KDB-917series

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number698003189R001CV Basic UDI-DIDate19 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Rollator
Model / Reference
KDBWG917B-A, KDBWG917B-B, KDBWG917C-A, KDBWG917C-B,KDBWG917D, KDBWG917E, KDBWG917F, KDBWG917G, KDBWG917H, KDBWG917I, KDB-917series
Primary DI / UDI-DI
06980031892727
Basic UDI-DI
698003189R001CV
EMDN Code
Y120606 Wheeled walker
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000055485
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Zhongshan KDB Health Solutions Co. Ltd.

See all devices from Zhongshan KDB Health Solutions 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