eudamed_udi Primary ID: M368FR601U92051

Lumex (UDI M368FR601U92051)

Manufactured by GF Health Products, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lumex (Model/Catalog Number: FR601U9205) is a medical device manufactured by GF Health Products, Inc.. This product is indexed under FDA Product Code / Category Classification V080202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FR601U9205
Product Code / EMDN: V080202
Device Name: Clinical Care Recliners
Database Sync Date: 2026-08-09 16:29:23

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 Lumex?

The registered manufacturer of record for Lumex is GF Health Products, Inc..

What is the Primary UDI-DI identifier for Lumex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M368FR601U92051.

What classification code is assigned to this device?

This device is registered under product classification code V080202.

Similar Classification Devices (V080202)

Other Devices by GF Health Products, Inc.

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