Bernafon 186038
Bernafon 186038 is a Class II device made by Bernafon, Inc., listed in FDA GUDID since 20 Aug 2018 (UDI-DI 05711584084403), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05711584084403 | Date20 Aug 2018 | StatusListed |
Official records
- AccessGUDID record 05711584084403
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bernafon
- Generic name
- Air-conduction hearing aid, in-the-ear
- Model / reference
- 186038
- Primary DI / UDI-DI
- 05711584084403
- FDA product code
- KLW, OSM
- GMDN term
- Air-conduction hearing aid, in-the-ear
- Device class
- Class II
- Regulation number
- 874.3400, 874.3305
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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