KINDaluna 1400

by audifon GmbH & Co. KG 3 variants

Ref 023175-A744-312-1720, 023175-A744-313-1720Model 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-023175-A744-312-17206R Basic UDI-DI	Date10 Apr 2026Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference: Hearing aid, 023175-A744-312-1720, 023175-A744-313-1720

Primary DI / UDI-DI: D-023175-A744-312-17206R, D-023175-A744-313-172076
Basic UDI-DI: B-023175-A744-312-17206R, B-023175-A744-313-172076
EMDN Code: Y2145060102 Behind-the-ear hearing aids with receiver in the canal (ric, rite)

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000008355

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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