Fuse (UDI FDEMO-F7528)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Fuse (Model/Catalog Number: FDEMO-F7528) 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: FDEMO-F7528
Product Code / EMDN: FDF
Device Name: Colonoscope
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 FDEMO-F7528.

What classification code is assigned to this device?

This device is registered under product classification code FDF.

Similar Classification Devices (FDF)

Other Devices by ENDOCHOICE, INC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint