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Nart Access Engelli̇ Plaj Sandalyesi̇

by Nartli̇ft Engelli̇ Ve Yaşli Asansörleri̇ Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Ref NART500

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 Number86835816092NARTSNDC7 Basic UDI-DI 08683581609217UDI-DIDate7 Jul 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  • Withdrawn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
Nart Access
Model / Reference
NART500
Primary DI / UDI-DI
08683581609217
Basic UDI-DI
86835816092NARTSNDC7
Direct Marketing DI
08683581609217
EMDN Code
Y0999 Personal care aids - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000052707

Other devices from Nartli̇ft Engelli̇ Ve Yaşli Asansörleri̇ Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

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