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gudid Primary ID: NS-901

NeuroSENSE (UDI NS-901)

Manufactured by Neurowave Systems Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeuroSENSE - Primary ID NS-901

Device Regulatory Overview

The NeuroSENSE (Model/Catalog Number: NS-901) is a medical device manufactured by Neurowave Systems Inc.. This product is indexed under FDA Product Code / Category Classification OLW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NS-901
Product Code / EMDN
OLW
Device Name
Database Sync Date
2026-08-09 09:06:29

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of NeuroSENSE?

The registered manufacturer of record for NeuroSENSE is Neurowave Systems Inc..

What is the Primary UDI-DI identifier for NeuroSENSE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NS-901.

What classification code is assigned to this device?

This device is registered under product classification code OLW.

Similar Classification Devices (OLW)

Other Devices by Neurowave Systems Inc.

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