Phonak Audéo P30-RT
EUDAMEDFDA UDIClass IIa (EU MDR)
by Sonova AG
Identity
- Trade Name
- Phonak Audéo P30-RT EUDAMEDPhonak Brand FDA UDI
- Generic Name
- Air-conduction hearing aid, receiver-in-canal FDA UDI
- Device Name
- Sonova RIC hearing aids EUDAMEDPhonak Audéo P30-RT (champagne) FDA UDI
- Model / Reference
- Sonova RIC hearing aids EUDAMED050-0795-P5 EUDAMEDFDA UDI
- Description
- Phonak Audéo P30-RT (champagne) FDA UDI
Identifiers
- Catalog Number
- 050-0795-P5 FDA UDI
- Primary DI / UDI-DI
- 07613389352283 EUDAMEDFDA UDI
- Basic UDI-DI
- 07613389RICWJ 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
- Austria 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
No
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
Yes
Category: Air-conduction hearing aid, receiver-in-canal
Phonak Audéo P30-RT by Sonova AG — 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
- HA VIO E156 T BC LI GPH — WSAUD A/S · Class IIa
- HANSATON — Hansaton Akustik GmbH · Class II
- AMPLIFON — Starkey Laboratories Inc. · Class II
- NUEAR — Starkey Laboratories Inc. · Class II
- HA AMPLI-MINI R 3 AX 312 BLK — WSAUD A/S · Class IIa
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 07613389RICWJ | 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
- Sonova AG
- EUDAMED SRN
- CH-MF-000015958
- Authorised Representative
- Sonova Deutschland GmbH DE-AR-000006322
Sources (2)
- EUDAMED 21d47064-2bd1-4fc1-8a1c-784654a36b8e 61 fields · synced Jul 10, 2026
- FDA UDI 8238ed45-191a-4d2c-a027-7acbfef92920 35 fields · synced May 25, 2026