GUDIDData
gudid Primary ID: B9630082020

BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS (UDI B9630082020)

Manufactured by EB NEURO SPA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS - Primary ID B9630082020

Device Regulatory Overview

The BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS (Model/Catalog Number: B9630082020) is a medical device manufactured by EB NEURO SPA. This product is indexed under FDA Product Code / Category Classification GWL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
B9630082020
Product Code / EMDN
GWL
Device Name
64 channels patient-interface for EEG amplifier
Database Sync Date
2026-08-09 09:04:29

Full Regulatory Attributes

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{
    "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 BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS?

The registered manufacturer of record for BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS is EB NEURO SPA.

What is the Primary UDI-DI identifier for BE PLUS LTM PLUG-IN HEADBOX, 64-CHANNELS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9630082020.

What classification code is assigned to this device?

This device is registered under product classification code GWL.

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