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Test band

EUDAMEDFDA UDI

Class I (EU MDR)

Ref M50104

by Oticon Medical AB

Identity

Trade Name
Test band EUDAMED
Ponto FDA UDI
Generic Name
Head-worn bone-conduction hearing aid FDA UDI
Device Name
Softband EUDAMED
Test band FDA UDI
Model / Reference
M50104 EUDAMEDFDA UDI
Description
Test band FDA UDI

Identifiers

Catalog Number
M50104 FDA UDI
Primary DI / UDI-DI
05712149000289 EUDAMEDFDA UDI
Basic UDI-DI
57121491000386 EUDAMED
FDA Product Code
LXB FDA UDI
EMDN Code
Y214599 HEARING AIDS - OTHER EUDAMED
GMDN Term
Head-worn bone-conduction hearing aid FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
874.3302 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Test band by Oticon Medical AB — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oticon Medical AB
EUDAMED SRN
SE-MF-000000724

Sources (2)

  • EUDAMED cf0eb054-7a01-4d62-941c-d6668d6151bf 61 fields · synced Jun 18, 2026
  • FDA UDI c507743f-c036-48de-9ec8-8cbea4a38e69 35 fields · synced May 29, 2026