GN ReSound 21176400
GN ReSound 21176400 is a Class I device made by Gn Hearing A/S, listed in FDA GUDID since 28 Aug 2019 (UDI-DI 05708296173112), registry data as of 2 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05708296173112 | Date28 Aug 2019 | StatusListed |
Official records
- AccessGUDID record 05708296173112
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- GN ReSound
- Generic name
- Air-conduction hearing aid, canal
- Model / reference
- 21176400
- Primary DI / UDI-DI
- 05708296173112
- FDA product code
- LRB, KLW
- GMDN term
- Air-conduction hearing aid, canal
- Device class
- Class I
- Regulation number
- 874.3300, 874.3400
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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