NeXus-Q32 2.0
NeXus-Q32 2.0 is a multiple physiological signal amplifier (FDA Class II; FDA product code HCC, Device, Biofeedback) made by Mind Media Europe B.V., registered in EUDAMED and listed in FDA GUDID since 19 Jul 2021 (UDI-DI 08719481550004), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number08719481550004 | Date19 Jul 2021 | StatusListed |
| European Union | CE/MDR EUDAMED | Number— | Date— | StatusActive |
Official records
- EUDAMED public site
- AccessGUDID record 08719481550004
Across registries
- EUDAMED Active
- FDA GUDID UDI-DI 08719481550004 listed 19 Jul 2021 Listed
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- NeXus-Q32
- Generic name
- Multiple physiological signal amplifier
- Model / reference
- 2.0
- Primary DI / UDI-DI
- 08719481550004
- FDA product code
- HCC
- GMDN term
- Multiple physiological signal amplifier
- Device class
- Class II
- Regulation number
- 882.5050
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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