NeXus-Q32

FDA UDI

Class II (US FDA UDI)

by Mind Media Europe B.V.

Identity

Trade Name: NeXus-Q32 FDA UDI
Generic Name: Multiple physiological signal amplifier FDA UDI
Device Name: The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.g. EEG, surface EMG or ECG) from humans, regardless of any specific medical indication, by medical/research professionals. FDA UDI
Model / Reference: 3.0 FDA UDI
Description: The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.g. EEG, surface EMG or ECG) from humans, regardless of any specific medical indication, by medical/research professionals. FDA UDI

Identifiers

Primary DI / UDI-DI: 08719481550400 FDA UDI
FDA Product Code: HCC FDA UDI
GMDN Term: Multiple physiological signal amplifier FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.5050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Multiple physiological signal amplifier

NeXus-Q32 by Mind Media Europe B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Mind Media Europe B.V.

Sources (1)

FDA UDI 5afac274-ad2e-4b73-83f9-b98e9077ac90 33 fields · synced Jun 9, 2026