gudid
Primary ID: LS-FSC330-G7522
Fuse (UDI LS-FSC330-G7522)
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 LS-FSC330-G7522
Device Regulatory Overview
The Fuse (Model/Catalog Number: LS-FSC330-G7522) is a medical device manufactured by ENDOCHOICE, INC.. This product is indexed under FDA Product Code / Category Classification FDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LS-FSC330-G7522
- Product Code / EMDN
- FDF
- Device Name
- Colonoscope
- Database Sync Date
- 2026-08-09 09:12:11
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 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 LS-FSC330-G7522.
What classification code is assigned to this device?
This device is registered under product classification code FDF.
Similar Classification Devices (FDF)
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