pma Primary ID: P880001

FLUOREX (TM) 600 (FLURSILFOCON A) (UDI P880001)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FLUOREX (TM) 600 (FLURSILFOCON A) (Model/Catalog Number: Unspecified) is a medical device manufactured by G.T. Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: HQD
Device Name: Lens, contact (other material) - daily
Database Sync Date: 2026-08-09 10:04:44

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 FLUOREX (TM) 600 (FLURSILFOCON A)?

The registered manufacturer of record for FLUOREX (TM) 600 (FLURSILFOCON A) is G.T. Laboratories, Inc..

What is the Primary UDI-DI identifier for FLUOREX (TM) 600 (FLURSILFOCON A)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P880001.

What classification code is assigned to this device?

This device is registered under product classification code HQD.

Similar Classification Devices (HQD)

Other Devices by G.T. Laboratories, Inc.

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