NeXus-Q32

GUDID 08719481550400

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.

Mind Media B.V.

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• Primary Device ID: 08719481550400
• NIH Device Record Key: 5afac274-ad2e-4b73-83f9-b98e9077ac90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeXus-Q32
• Version Model Number: 3.0
• Company DUNS: 489837775
• Company Name: Mind Media 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	08719481550400 [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: 2023-02-16
• Device Publish Date: 2023-02-08

On-Brand Devices [NeXus-Q32]

• 08719481550004: The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.g. EEG, surface
• 08719481550400: The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.g. EEG, surface