gudid Primary ID: FGC13200 0000

Carex (UDI FGC13200 0000)

Manufactured by Drive Devilbiss Healthcare

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Carex (Model/Catalog Number: FGC13200 0000) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification BTK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FGC13200 0000
Product Code / EMDN: BTK
Device Name: Premium Chin Strap
Database Sync Date: 2026-08-09 09:00:33

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 Carex?

The registered manufacturer of record for Carex is Drive Devilbiss Healthcare.

What is the Primary UDI-DI identifier for Carex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FGC13200 0000.

What classification code is assigned to this device?

This device is registered under product classification code BTK.

Similar Classification Devices (BTK)

Other Devices by Drive Devilbiss Healthcare

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