gudid
Primary ID: FSG-2500-ST-R
Fuse (UDI FSG-2500-ST-R)
Manufactured by ENDOCHOICE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fuse - Primary ID FSG-2500-ST-R
Device Regulatory Overview
The Fuse (Model/Catalog Number: FSG-2500-ST-R) is a medical device manufactured by ENDOCHOICE, INC.. This product is indexed under FDA Product Code / Category Classification FDS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FSG-2500-ST-R
- Product Code / EMDN
- FDS
- Device Name
- Gastroscope
- Database Sync Date
- 2026-08-09 09:12:11
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Fuse?
The registered manufacturer of record for Fuse is ENDOCHOICE, INC..
What is the Primary UDI-DI identifier for Fuse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FSG-2500-ST-R.
What classification code is assigned to this device?
This device is registered under product classification code FDS.
Similar Classification Devices (FDS)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint