gudid
Primary ID: B9800078002
BE PLUS PRO [STANDARD] (UDI B9800078002)
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 PRO [STANDARD] - Primary ID B9800078002
Device Regulatory Overview
The BE PLUS PRO [STANDARD] (Model/Catalog Number: B9800078002) 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
- B9800078002
- Product Code / EMDN
- GWL
- Device Name
- BE PLUS PRO [STANDARD] is an active medical device aimed to collect and record physiological signals from human body.It includes amplifier and accessories.
- Database Sync Date
- 2026-08-09 09:04:29
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BE PLUS PRO [STANDARD]?
The registered manufacturer of record for BE PLUS PRO [STANDARD] is EB NEURO SPA.
What is the Primary UDI-DI identifier for BE PLUS PRO [STANDARD]?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9800078002.
What classification code is assigned to this device?
This device is registered under product classification code GWL.
Similar Classification Devices (GWL)
Other Devices by EB NEURO SPA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint