gudid
Primary ID: 13-41000-0001
Electrodes (UDI 13-41000-0001)
Manufactured by DYMEDIX DIAGNOSTICS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Electrodes - Primary ID 13-41000-0001
Device Regulatory Overview
The Electrodes (Model/Catalog Number: 13-41000-0001) is a medical device manufactured by DYMEDIX DIAGNOSTICS, INC.. This product is indexed under FDA Product Code / Category Classification GXY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13-41000-0001
- Product Code / EMDN
- GXY
- Device Name
- Dual Wired EMG Electrode 120"
- Database Sync Date
- 2026-08-09 09:31:20
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 Electrodes?
The registered manufacturer of record for Electrodes is DYMEDIX DIAGNOSTICS, INC..
What is the Primary UDI-DI identifier for Electrodes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13-41000-0001.
What classification code is assigned to this device?
This device is registered under product classification code GXY.
Similar Classification Devices (GXY)
Other Devices by DYMEDIX DIAGNOSTICS, INC.
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