gudid
Primary ID: DGF-2318RT
Endoch (UDI DGF-2318RT)
Manufactured by Endoch Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Endoch - Primary ID DGF-2318RT
Device Regulatory Overview
The Endoch (Model/Catalog Number: DGF-2318RT) is a medical device manufactured by Endoch Inc. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DGF-2318RT
- Product Code / EMDN
- GEI
- Device Name
- GRASPING FORCEP
- Database Sync Date
- 2026-08-09 09:01:09
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 Endoch?
The registered manufacturer of record for Endoch is Endoch Inc.
What is the Primary UDI-DI identifier for Endoch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DGF-2318RT.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by Endoch Inc
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