gudid
Primary ID: DL844003
LF (UDI DL844003)
Manufactured by Liebel-Flarsheim Company LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LF - Primary ID DL844003
Device Regulatory Overview
The LF (Model/Catalog Number: DL844003) is a medical device manufactured by Liebel-Flarsheim Company LLC. This product is indexed under FDA Product Code / Category Classification IZQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DL844003
- Product Code / EMDN
- IZQ
- Device Name
- OptiVantage Dual-Head CT Contrast Delivery System, Demo Loan
- Database Sync Date
- 2026-08-09 10:00:18
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 LF?
The registered manufacturer of record for LF is Liebel-Flarsheim Company LLC.
What is the Primary UDI-DI identifier for LF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DL844003.
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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