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Joleti

by Yelken Aydinlatma Enerji̇ Isitma Si̇stemleri̇ Mühendi̇sli̇k Hi̇zmetleri̇ İth. İhr. San. Ti̇c. Ltd. Şti̇. 2 variants

Ref L400A180

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 Number86837810874DGBCK Basic UDI-DI 86837810874190UDI-DIDate9 Aug 2022RegisteredStatusActive

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  • Withdrawn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
Disability Grab Bar
Model / Reference
L400A180
Primary DI / UDI-DI
86837810874190
Basic UDI-DI
86837810874DGBCK
EMDN Code
Y181803 Handrails
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
TR-MF-000026673

Other devices from Yelken Aydinlatma Enerji̇ Isitma Si̇stemleri̇ Mühendi̇sli̇k Hi̇zmetleri̇ İth. İhr. San. Ti̇c. Ltd. Şti̇.

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