gudid
Primary ID: B9800086013
STM9000 STANDARD_BI (UDI B9800086013)
Manufactured by EB NEURO SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STM9000 STANDARD_BI - Primary ID B9800086013
Device Regulatory Overview
The STM9000 STANDARD_BI (Model/Catalog Number: B9800086013) is a medical device manufactured by EB NEURO SPA. This product is indexed under FDA Product Code / Category Classification GWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B9800086013
- Product Code / EMDN
- GWF
- Device Name
- Magnetic neural stimulation system. (Power supply voltage: 230VAC).
- 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 STM9000 STANDARD_BI?
The registered manufacturer of record for STM9000 STANDARD_BI is EB NEURO SPA.
What is the Primary UDI-DI identifier for STM9000 STANDARD_BI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9800086013.
What classification code is assigned to this device?
This device is registered under product classification code GWF.
Similar Classification Devices (GWF)
Other Devices by EB NEURO SPA
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