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SoniTon

EUDAMED

Class IIa (EU MDR)

Ref 257559Model HI (BTE)

by SBO Hearing A/S

Identity

Trade Name
SoniTon EUDAMED
Model / Reference
HI (BTE) EUDAMED
257559 EUDAMED

Identifiers

Primary DI / UDI-DI
05714464120581 EUDAMED
Basic UDI-DI
57144640-HI-00053-RB EUDAMED
EMDN Code
Y2145060102 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE CANAL (RIC, RITE) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark 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, receiver-in-canal

SoniTon by Sbo Hearing A/S — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, receiver-in-canal.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
SBO Hearing A/S
EUDAMED SRN
DK-MF-000001270

Sources (1)

  • EUDAMED 8f802338-8fbc-4f85-865a-2130ebae8edf 61 fields · synced May 29, 2026