Unitron 058-5236
Unitron 058-5236 is a Class II device made by Unitron Hearing Division, listed in FDA GUDID since 4 Dec 2020 (UDI-DI 07613389303292), registry data as of 23 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 | Number07613389303292 | Date4 Dec 2020 | StatusListed |
Official records
- AccessGUDID record 07613389303292
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Unitron
- Generic name
- Audiometric/hearing device software
- Model / Ref / Catalog
- 058-5236
- Primary DI / UDI-DI
- 07613389303292
- FDA product code
- OSM
- GMDN term
- Audiometric/hearing device software
- Device class
- Class II
- Regulation number
- 874.3305
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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