MEDRAD Stellant FLEX CT Injection System with Certegra Workstation (UDI Stellant FLEX)
Manufactured by BAYER MEDICAL CARE INC.
Device Regulatory Overview
The MEDRAD Stellant FLEX CT Injection System with Certegra Workstation (Model/Catalog Number: Stellant FLEX) is a medical device manufactured by BAYER MEDICAL CARE INC.. This product is indexed under FDA Product Code / Category Classification IZQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Stellant FLEX
- Product Code / EMDN
- IZQ
- Device Name
- SYSTEM,DUAL,STELLANT,FLEX (85577026)
- Database Sync Date
- 2026-08-09 09:50:08
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 MEDRAD Stellant FLEX CT Injection System with Certegra Workstation?
The registered manufacturer of record for MEDRAD Stellant FLEX CT Injection System with Certegra Workstation is BAYER MEDICAL CARE INC..
What is the Primary UDI-DI identifier for MEDRAD Stellant FLEX CT Injection System with Certegra Workstation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Stellant FLEX.
What classification code is assigned to this device?
This device is registered under product classification code IZQ.
Similar Classification Devices (IZQ)
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