gudid
Primary ID: EndyGel 350 ml
EndyGel (UDI EndyGel 350 ml)
Manufactured by ENDYMED MEDICAL LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EndyGel - Primary ID EndyGel 350 ml
Device Regulatory Overview
The EndyGel (Model/Catalog Number: EndyGel 350 ml) is a medical device manufactured by ENDYMED MEDICAL LTD. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EndyGel 350 ml
- Product Code / EMDN
- GYB
- Device Name
- EndyGel is an Electroconductive gel media used with external electrode to reduce the impedance (resistance to alternating current) of the contract between the electrode surface and the skin.
- Database Sync Date
- 2026-08-09 09:18:18
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 EndyGel?
The registered manufacturer of record for EndyGel is ENDYMED MEDICAL LTD.
What is the Primary UDI-DI identifier for EndyGel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EndyGel 350 ml.
What classification code is assigned to this device?
This device is registered under product classification code GYB.
Similar Classification Devices (GYB)
Other Devices by ENDYMED MEDICAL LTD
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