gudid
Primary ID: B9800066801
NeMus 2 + (UDI B9800066801)
Manufactured by EB NEURO SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeMus 2 + - Primary ID B9800066801
Device Regulatory Overview
The NeMus 2 + (Model/Catalog Number: B9800066801) is a medical device manufactured by EB NEURO SPA. This product is indexed under FDA Product Code / Category Classification GWJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B9800066801
- Product Code / EMDN
- GWJ
- Device Name
- EEG/EMG/EP System
- 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 NeMus 2 +?
The registered manufacturer of record for NeMus 2 + is EB NEURO SPA.
What is the Primary UDI-DI identifier for NeMus 2 +?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B9800066801.
What classification code is assigned to this device?
This device is registered under product classification code GWJ.
Similar Classification Devices (GWJ)
Other Devices by EB NEURO SPA
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