← Back to catalogue

Ha Allure Arrd1 110 Gbrn

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 21029006Model RICRef 21048826

by Wsaud A/S

Identity

Trade Name
HA ALLURE ARRD1 110 GBRN EUDAMED
HA ALLURE ARRD2 110 GBRN EUDAMED
Widex FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-canal FDA UDI
Device Name
HA ALLURE ARRD1 110 GBRN FDA UDI
Model / Reference
RIC EUDAMED
21029006 EUDAMED
21048826 EUDAMED
ALLURE ARRD1 110 FDA UDI
Description
HA ALLURE ARRD1 110 GBRN FDA UDI

Identifiers

Catalog Number
21029006 FDA UDI
Primary DI / UDI-DI
05714880209358 EUDAMEDFDA UDI
05714880292374 EUDAMED
Basic UDI-DI
5714880-WSA-66-15-5M EUDAMED
5714880-WSA-76-15-62 EUDAMED
FDA Product Code
OSM FDA UDI
EMDN Code
Y2145060102 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE CANAL (RIC, RITE) EUDAMED
GMDN Term
Air-conduction hearing aid, receiver-in-canal FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
874.3305 FDA UDI
Market of Registration
Germany 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Air-conduction hearing aid, receiver-in-canal

Ha Allure Arrd1 110 Gbrn by Wsaud A/S — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Wsaud A/S
EUDAMED SRN
DK-MF-000015974

Sources (3)

  • EUDAMED 542ef05c-1f23-487a-9c9b-7a0f0659444d 61 fields · synced Jul 8, 2026
  • FDA UDI 8d3516b8-88c1-4625-beba-ac52809cae80 35 fields · synced May 29, 2026
  • EUDAMED d2228a7f-a6af-4315-bdc9-068f5ed31093 61 fields · synced Jun 19, 2026