gudid
Primary ID: HEMFSM10
HEMOSPHERE FORESIGHT MODULE (UDI HEMFSM10)
Manufactured by Edwards Lifesciences LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HEMOSPHERE FORESIGHT MODULE - Primary ID HEMFSM10
Device Regulatory Overview
The HEMOSPHERE FORESIGHT MODULE (Model/Catalog Number: HEMFSM10) 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
- HEMFSM10
- Product Code / EMDN
- MUD
- Device Name
- HEMOSPHERE FORESIGHT MODULE
- 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 HEMOSPHERE FORESIGHT MODULE?
The registered manufacturer of record for HEMOSPHERE FORESIGHT MODULE is Edwards Lifesciences LLC.
What is the Primary UDI-DI identifier for HEMOSPHERE FORESIGHT MODULE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HEMFSM10.
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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