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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

023174-A743-332-1720 — Class IIa MDD by audifon GmbH & Co. KG

MD Atlas
audifon GmbH & Co. KG

EUDAMED last updated this device on Apr 10, 2026

023174-A743-332-1720

B-023174-A743-332-17205F

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: audifon GmbH & Co. KG
UDI-DI code: D-023174-A743-332-17205F
Reference / catalog number: 023174-A743-332-1720

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Manufacturer information

Organization name: audifon GmbH & Co. KG
SRN: DE-MF-000008355
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Mar 21, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-023174-A743-332-17205F
Basic UDI-DI: B-023174-A743-332-17205F
Reference / catalog number: 023174-A743-332-1720
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: KINDaluna 1100 -- silbergrau-metallic
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y2145060101BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification