gudid
Primary ID: B9700078001
BE PLUS PRO LIGHT (UDI B9700078001)
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 LIGHT - Primary ID B9700078001
Device Regulatory Overview
The BE PLUS PRO LIGHT (Model/Catalog Number: B9700078001) 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
- B9700078001
- Product Code / EMDN
- GWL
- Device Name
- Acquisition unit
- 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 LIGHT?
The registered manufacturer of record for BE PLUS PRO LIGHT is EB NEURO SPA.
What is the Primary UDI-DI identifier for BE PLUS PRO LIGHT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9700078001.
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