NeXus Software 1.0.204.6
NeXus Software 1.0.204.6 is a Class II device made by Mind Media Europe B.V., listed in FDA GUDID since 19 Jul 2021 (UDI-DI 08719481550332), 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 | Number08719481550332 | Date19 Jul 2021 | StatusListed |
Official records
- AccessGUDID record 08719481550332
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NeXus Software
- Generic name
- Biofeedback system application software
- Model / reference
- 1.0.204.6
- Primary DI / UDI-DI
- 08719481550332
- FDA product code
- HCC
- GMDN term
- Biofeedback system application software
- Device class
- Class II
- Regulation number
- 882.5050
- GUDID distribution status
- In Commercial Distribution
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