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Koj

EUDAMED

Class IIa (EU MDR)

Ref 235953Model HI (BTE)Ref 234411

by SBO Hearing A/S

Identity

Trade Name
KOJ EUDAMED
Model / Reference
HI (BTE) EUDAMED
235953 EUDAMED
234411 EUDAMED

Identifiers

Primary DI / UDI-DI
05714464046102 EUDAMED
05714464037384 EUDAMED
Basic UDI-DI
57144640-HI-00052-R8 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
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, behind-the-ear

Koj by Sbo Hearing A/S — 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
SBO Hearing A/S
EUDAMED SRN
DK-MF-000001270

Sources (2)

  • EUDAMED 55b783c0-6814-467b-a8d3-bcca67381a34 61 fields · synced Jul 28, 2026
  • EUDAMED e05acbf1-29e9-4f82-866e-db856801e929 61 fields · synced May 18, 2026