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Cane

by Nova Orthopedic & Rehabilitation Appliance Inc. 23 variants

Ref 203000-A500-E029

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 Number471989092CANE2030SV Basic UDI-DI 04719890922526UDI-DIDate24 Jun 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  • Withdrawn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
Cane
Model / Reference
203000-A500-E029
Primary DI / UDI-DI
04719890922526
Basic UDI-DI
471989092CANE2030SV
Direct Marketing DI
04719890922526
EMDN Code
Y120399 Walking devices, one-handed operation - other
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
TW-MF-000024107
Authorised representative
KOMAS Medical Technology GmbH DE-AR-000045617

Other devices from Nova Orthopedic & Rehabilitation Appliance Inc.

See all devices from Nova Orthopedic & Rehabilitation Appliance Inc. →

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