Skip to content

kami ITE V50

by audifon GmbH & Co. KG 6 variants

Ref 023301-9263-315-357Model Hearing aid

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-023301-9263-315-357BX Basic UDI-DI D-023301-9263-315-357BXUDI-DIDate2 Dec 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Hearing aid, 023301-9263-315-357
Primary DI / UDI-DI
D-023301-9263-315-357BX
Basic UDI-DI
B-023301-9263-315-357BX
EMDN Code
Y2145060201 Hearing aid in the-ear (ite)
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008355

Other devices from audifon GmbH & Co. KG

  • rega XS

    Class IIa

  • Power

    Class IIa

  • rega R

    Class IIa

  • He-S

    Class IIa

  • He-P

    Class IIa

  • offen

    Class IIa

See all devices from audifon GmbH & Co. KG →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No