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beat FS 1-RT13 SP (metallic anthracite)

EUDAMED

Class IIa (EU MDR)

Ref 050-6880-UCModel Sonova BTE hearing aids

by Sonova AG

Identity

Trade Name
beat FS 1-RT13 SP (metallic anthracite) EUDAMED
Device Name
Sonova BTE hearing aids EUDAMED
Model / Reference
Sonova BTE hearing aids EUDAMED
050-6880-UC EUDAMED

Identifiers

Primary DI / UDI-DI
07613389736540 EUDAMED
Basic UDI-DI
07613389BTEV7 EUDAMED
EMDN Code
Y2145060101 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE) 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

Category: Air-conduction hearing aid, behind-the-ear

beat FS 1-RT13 SP (metallic anthracite) by Sonova AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, behind-the-ear.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Sonova AG
EUDAMED SRN
CH-MF-000015958
Authorised Representative
Sonova Deutschland GmbH DE-AR-000006322

Sources (1)

  • EUDAMED 3860264f-90df-4357-868d-17e5aae7c439 61 fields · synced Jul 25, 2026