# NeXus-Q32 2.0

> Active: European Union. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/nexus-q32-2-0>
- Manufacturer: [Mind Media Europe B.V.](https://devicerts.com/manufacturers/mind-media-europe-b-v) (FDA registration: United States)
- Device class: Class II (US FDA)
- FDA product code: HCC
- GMDN: Multiple physiological signal amplifier (32521)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 08719481550004 · listed 2021-07-19 · status: Listed (GUDID: in commercial distribution)
- **EUDAMED** · CE/MDR · European Union · status: Active

## Recalls

No recall on record.

## Identity

- Trade name: NeXus-Q32 [FDA GUDID (AccessGUDID)]
- Generic name: Multiple physiological signal amplifier [FDA GUDID (AccessGUDID)]
- Model / reference: 2.0 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 08719481550004 [FDA GUDID (AccessGUDID)]
- FDA product code: HCC [FDA GUDID (AccessGUDID)]
- GMDN term: Multiple physiological signal amplifier (32521) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 882.5050 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- MRI safety: MR Unsafe [FDA GUDID (AccessGUDID)]

## Properties

- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Premarket exempt: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: NeXus-Q32 2.0, Mind Media Europe B.V. deviCERTS medical device catalogue. https://devicerts.com/devices/nexus-q32-2-0 (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/nexus-q32-2-0.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/nexus-q32-2-0
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.