gudid
Primary ID: DX500
NerveOTX (UDI DX500)
Manufactured by DOMINO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NerveOTX - Primary ID DX500
Device Regulatory Overview
The NerveOTX (Model/Catalog Number: DX500) is a medical device manufactured by DOMINO SRL. This product is indexed under FDA Product Code / Category Classification NGX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DX500
- Product Code / EMDN
- NGX
- Device Name
- The NerveOTX DX500 is a muscle stimulator. The device comes with a menu to navigate between different stimulation programs. The Stimulation Programs have been subdivided in menus and submenus to facilitate use for various types of uses.
- Database Sync Date
- 2026-08-09 09:05:06
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 NerveOTX?
The registered manufacturer of record for NerveOTX is DOMINO SRL.
What is the Primary UDI-DI identifier for NerveOTX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DX500.
What classification code is assigned to this device?
This device is registered under product classification code NGX.
Similar Classification Devices (NGX)
Other Devices by DOMINO SRL
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