NeXus Q24

GUDID 08719481550165

The NeXus | Q24 is designed for medical use, not restricted to a specific medical indication, for acquisition of (electro)-physiological signals (e.g. EEG, EMG or ECG). The product is intended to be used by medical/access professionals in a laboratory setup or medical office, or to be set-up in such an environment after which the subject/patient can be sent out while signal acquisition continues on memory. The NeXus Q24 is not intended for use in diagnosis, nor in critical and/or life supporting applications. The NeXus Q24 is intended for use on humans. The NeXus Q24 is intended to be used with approved NeXus accessories only. Specifically, (active) sensors intended to measure specific physiological signals, shall be designed in accordance with the specifications of the NeXus.

Mind Media Europe B.V.

Multiple physiological signal amplifier

• Primary Device ID: 08719481550165
• NIH Device Record Key: f8a9b3a0-3e3e-4a86-94a7-1975f48b61a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeXus Q24
• Version Model Number: 1.0
• Company DUNS: 494765181
• Company Name: Mind Media Europe B.V.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08719481550165 [Primary]

FDA Product Code

• HCC: Device, Biofeedback

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-11
• Device Publish Date: 2025-12-03