gudid
Primary ID: Mass Casualty Assembly
Flotec (UDI Mass Casualty Assembly)
Manufactured by FLOTEC INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flotec - Primary ID Mass Casualty Assembly
Device Regulatory Overview
The Flotec (Model/Catalog Number: Mass Casualty Assembly) is a medical device manufactured by FLOTEC INC. This product is indexed under FDA Product Code / Category Classification BYX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Mass Casualty Assembly
- Product Code / EMDN
- BYX
- Device Name
- Database Sync Date
- 2026-08-09 09:06:29
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 Flotec?
The registered manufacturer of record for Flotec is FLOTEC INC.
What is the Primary UDI-DI identifier for Flotec?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Mass Casualty Assembly.
What classification code is assigned to this device?
This device is registered under product classification code BYX.
Similar Classification Devices (BYX)
Other Devices by FLOTEC INC
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