gudid
Primary ID: FSESNS
ForeSight (UDI FSESNS)
Manufactured by Edwards Lifesciences LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ForeSight - Primary ID FSESNS
Device Regulatory Overview
The ForeSight (Model/Catalog Number: FSESNS) 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
- FSESNS
- Product Code / EMDN
- MUD
- Device Name
- ForeSight Sensor Non-adhesive Small
- Database Sync Date
- 2026-08-09 09:04:21
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 ForeSight?
The registered manufacturer of record for ForeSight is Edwards Lifesciences LLC.
What is the Primary UDI-DI identifier for ForeSight?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FSESNS.
What classification code is assigned to this device?
This device is registered under product classification code MUD.
Similar Classification Devices (MUD)
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