gudid
Primary ID: EG-s
Endogel (UDI EG-s)
Manufactured by JORDCO INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Endogel - Primary ID EG-s
Device Regulatory Overview
The Endogel (Model/Catalog Number: EG-s) is a medical device manufactured by JORDCO INC. This product is indexed under FDA Product Code / Category Classification KJJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EG-s
- Product Code / EMDN
- KJJ
- Device Name
- Dental Root Canal Lubricating and Cleanser gel, 12 tubes per pack
- Database Sync Date
- 2026-08-09 09:49:19
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 Endogel?
The registered manufacturer of record for Endogel is JORDCO INC.
What is the Primary UDI-DI identifier for Endogel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EG-s.
What classification code is assigned to this device?
This device is registered under product classification code KJJ.
Similar Classification Devices (KJJ)
Other Devices by JORDCO INC
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