GUDIDData
gudid Primary ID: FSEO2004

FORESIGHT ELITE (UDI FSEO2004)

Manufactured by Edwards Lifesciences LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FORESIGHT ELITE - Primary ID FSEO2004

Device Regulatory Overview

The FORESIGHT ELITE (Model/Catalog Number: FSEO2004) is a medical device manufactured by Edwards Lifesciences LLC. This product is indexed under FDA Product Code / Category Classification MUD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FSEO2004
Product Code / EMDN
MUD
Device Name
FORESIGHT ELITE OXIMETER PREAMP CABLE, 4M
Database Sync Date
2026-08-09 09:04:21

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 FORESIGHT ELITE?

The registered manufacturer of record for FORESIGHT ELITE is Edwards Lifesciences LLC.

What is the Primary UDI-DI identifier for FORESIGHT ELITE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FSEO2004.

What classification code is assigned to this device?

This device is registered under product classification code MUD.

Programmatic Export

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

JSON API Endpoint