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Amplifon

EUDAMED

Class I (EU MDR)

Ref 211921Model Audioclip

by SBO Hearing A/S

Identity

Trade Name
Amplifon EUDAMED
Model / Reference
Audioclip EUDAMED
211921 EUDAMED

Identifiers

Primary DI / UDI-DI
05707131375902 EUDAMED
Basic UDI-DI
57144640-AC-00034-GH EUDAMED
EMDN Code
Y214580 HEARING AIDS OR HEARING DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class I 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

Amplifon by Sbo Hearing A/S — Class I — 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

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

Sources (1)

  • EUDAMED fc6bb6e8-6763-4568-a7ce-bb6d011e39d4 61 fields · synced Jun 19, 2026