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Padded Knee Sleeve - Ortho-tex - Large

by Chaneco Ltd

Ref KSP-O-LModel KSP

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 Number50561576KneeSleevePadDT Basic UDI-DIDate14 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Padded Knee Sleeve
Model / Reference
KSP, KSP-O-L
Primary DI / UDI-DI
05056157601145
Basic UDI-DI
50561576KneeSleevePadDT
EMDN Code
Y061299 Lower extremity orthoses - other
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
UK-MF-000043937
Authorised representative
UKALIA Limited XI-AR-000024526

Other devices from Chaneco Ltd

See all devices from Chaneco 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