gudid Primary ID: 10225786.FGX

LUCAS FILMS (UDI 10225786.FGX)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The LUCAS FILMS (Model/Catalog Number: 10225786.FGX) is a medical device manufactured by FGX INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification HQY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10225786.FGX
Product Code / EMDN: HQY
Device Name
Database Sync Date: 2026-08-09 09:00:32

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 LUCAS FILMS?

The registered manufacturer of record for LUCAS FILMS is FGX INTERNATIONAL INC..

What is the Primary UDI-DI identifier for LUCAS FILMS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10225786.FGX.

What classification code is assigned to this device?

This device is registered under product classification code HQY.

Similar Classification Devices (HQY)

Other Devices by FGX INTERNATIONAL INC.

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