← Back to catalogue
Ha Ampli-Connect R 4 Ax 312 Dbr
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 21015164Model RIC
by Wsaud A/S
Identity
- Trade Name
- HA AMPLI-CONNECT R 4 AX 312 DBR EUDAMEDAmplifon FDA UDI
- Generic Name
- Air-conduction hearing aid, receiver-in-canal FDA UDI
- Device Name
- Amplifon HA AMPLI-CONNECT R 4 AX 312 DBR Hearing aid FDA UDI
- Model / Reference
- RIC EUDAMED21015164 EUDAMEDampli-connect R 4 AX 312 FDA UDI
- Description
- Amplifon HA AMPLI-CONNECT R 4 AX 312 DBR Hearing aid FDA UDI
Identifiers
- Catalog Number
- 21015164 FDA UDI
- Primary DI / UDI-DI
- 05714880165951 EUDAMEDFDA UDI
- Basic UDI-DI
- 5714880-WSA-26-15-3Z 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
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
Ha Ampli-Connect R 4 Ax 312 Dbr by Wsaud A/S — Class IIa — 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5714880-WSA-26-15-3Z | 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 (2)
- EUDAMED 854ed799-6fd5-4c38-9480-8755dcf46594 61 fields · synced Jun 18, 2026
- FDA UDI d92e9e26-0786-4371-bce2-3c4828819ba2 35 fields · synced May 22, 2026