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KINDvaro 5700 nw

EUDAMED

Class IIa (EU MDR)

Ref 72047-KIN

by Starkey Laboratories Inc.

Identity

Trade Name
KINDvaro 5700 nw EUDAMED
Device Name
Genesis AI Custom EUDAMED
Model / Reference
72047-KIN EUDAMED

Identifiers

Primary DI / UDI-DI
00842318196422 EUDAMED
Basic UDI-DI
0842318172047UZ EUDAMED
EMDN Code
Y2145060203 HEARING AIDS COMPLETELY-IN-THE-CANAL (CIC) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

KINDvaro 5700 nw by Starkey Laboratories Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000014382
Authorised Representative
Starkey Laboratories (Germany) GmbH DE-AR-000010831

Sources (1)

  • EUDAMED b54d4e71-6baf-4a70-a33b-82462665c1a1 61 fields · synced Jun 19, 2026