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Hikoneb A103

by KARE MEDiKAL VE ANALiTiK CiH. SAN. VE TiC. LTD. STi. Türkiye EUDAMED

Ref M000481Model Hikoneb A103

EMDN R060101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08698934522020 Basic UDI-DIDate28 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Compressor Nebulizer
Model / Reference
Hikoneb A103, M000481
Primary DI / UDI-DI
08698934522020
Basic UDI-DI
B-08698934522020
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020956

Other devices from KARE MEDiKAL VE ANALiTiK CiH. SAN. VE TiC. LTD. STi.

See all devices from KARE MEDiKAL VE ANALiTiK CiH. SAN. VE TiC. LTD. STi. →

Properties & raw data

Show properties, registry sources and raw records
  • Administering Medicine
Other properties (10)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 3b080579-c633-47ac-8058-e3b625968c3a 61 fields · synced 22 Oct 2026