gudid
Primary ID: B9700063000
Flash Led Stimulator (UDI B9700063000)
Manufactured by EB NEURO SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flash Led Stimulator - Primary ID B9700063000
Device Regulatory Overview
The Flash Led Stimulator (Model/Catalog Number: B9700063000) is a medical device manufactured by EB NEURO SPA. This product is indexed under FDA Product Code / Category Classification GWE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B9700063000
- Product Code / EMDN
- GWE
- Device Name
- Flash Stimulator for EEG/EP/EMG
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Flash Led Stimulator?
The registered manufacturer of record for Flash Led Stimulator is EB NEURO SPA.
What is the Primary UDI-DI identifier for Flash Led Stimulator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9700063000.
What classification code is assigned to this device?
This device is registered under product classification code GWE.
Similar Classification Devices (GWE)
Other Devices by EB NEURO SPA
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