Ha Allure Arrd1 220 Ccrn
EUDAMEDFDA UDIClass IIa (EU MDR)
by Wsaud A/S
Identity
- Trade Name
- HA ALLURE ARRD1 220 CCRN EUDAMEDHA ALLURE ARRD2 220 CCRN EUDAMEDWidex FDA UDI
- Generic Name
- Air-conduction hearing aid, receiver-in-canal FDA UDI
- Device Name
- HA ALLURE ARRD1 220 CCRN FDA UDI
- Model / Reference
- RIC EUDAMED21028988 EUDAMED21048830 EUDAMEDALLURE ARRD1 220 FDA UDI
- Description
- HA ALLURE ARRD1 220 CCRN FDA UDI
Identifiers
- Catalog Number
- 21028988 FDA UDI
- Primary DI / UDI-DI
- 05714880209433 EUDAMEDFDA UDI05714880292336 EUDAMED
- Basic UDI-DI
- 5714880-WSA-66-15-5M EUDAMED5714880-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 EUDAMEDClass 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
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Air-conduction hearing aid, receiver-in-canal
Ha Allure Arrd1 220 Ccrn 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.
- SET CROS PURE CHARGE&GO PRL — Signia GmbH · Class IIa
- HA EVK E-FS-T USA 440 SLVGR — Widex A/S · Class IIa
- AGXO — Sbo Hearing A/S · Class IIa
- SoniTon UP6 312 trial — Sonova AG · Class IIa
- HANSATON — Hansaton Akustik GmbH · Class II
- PHONAK — Sonova AG · Class II
- AMPLIFON — Starkey Laboratories Inc. · Class II
- NUEAR — Starkey Laboratories Inc. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5714880-WSA-66-15-5M | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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 47f138e3-c9ca-4f83-9bbe-4f72726d8bba 61 fields · synced Jul 26, 2026
- FDA UDI 3f2bb5e8-5ec2-4ef5-841e-054715ca0f90 35 fields · synced May 30, 2026
- EUDAMED 6b0300fd-09dd-4e48-ad60-c22db609ccfd 61 fields · synced Jul 26, 2026