Skip to content

TAYA REST Axillary crutch

by Taya Medical Saglik Hizmetleri̇ Turizm Pazarlama Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi

Ref TY-REST

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number86850948434TYCRURB Basic UDI-DI 08685094843447UDI-DIDate22 Jan 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  • Withdrawn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
Crutch
Model / Reference
TY-REST
Primary DI / UDI-DI
08685094843447
Basic UDI-DI
86850948434TYCRURB
Direct Marketing DI
08685094843447
EMDN Code
Y120399 Walking devices, one-handed operation - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000050717

Other devices from Taya Medical Saglik Hizmetleri̇ Turizm Pazarlama Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi

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