LF (UDI 844210)

Manufactured by Liebel-Flarsheim Company LLC

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The LF (Model/Catalog Number: 844210) 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: 844210
Product Code / EMDN: IZQ
Device Name: OptiBolus, Bolus Shaping Software, International (Accessory)
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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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 844210.

What classification code is assigned to this device?

This device is registered under product classification code IZQ.

Similar Classification Devices (IZQ)

Other Devices by Liebel-Flarsheim Company LLC

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