NeXus-Q32 3.0
NeXus-Q32 3.0 is a Class II device made by Mind Media Europe B.V., listed in FDA GUDID since 8 Feb 2023 (UDI-DI 08719481550400), 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 | Number08719481550400 | Date8 Feb 2023 | StatusListed |
Official records
- AccessGUDID record 08719481550400
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NeXus-Q32
- Generic name
- Multiple physiological signal amplifier
- Model / reference
- 3.0
- Primary DI / UDI-DI
- 08719481550400
- 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
Similar devices
Other devices filed under FDA product code HCC (Device, Biofeedback).
- CLINICAL EMG MODEL 133 by Calnor of EL Paseo, Inc.
- NEUROINFINITI 2 SA7904 by Thought Technology Ltd.
- MYOMETER EMG BIOFEEDBACK DEVICE by Physio Technology, Inc.
- ORION BIOFEEDBACK DATA ACQUISITION by Self Regulation Systems, Inc.
- BIOFEEDBACK DEVICE by Verimed Holdings, Inc.
- MODEL BIOSTAR by Targus Concepts
- ORION PLATINUM by SRS Medical Systems, Inc.
- NEUROSEARCH-4 by Lexicor
- HR/BVP 100T HEART RATE MONITOR by THOUGHT TECHNOLOGY LTD.
- DEI MODEL 20 EEG by Discovery Engineering Intl., Inc.