gudid Primary ID: 5001001

Titanium-Vocal-Fold-Medial-Implant (UDI 5001001)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Titanium-Vocal-Fold-Medial-Implant (Model/Catalog Number: 5001001) is a medical device manufactured by Heinz Kurz GmbH. This product is indexed under FDA Product Code / Category Classification KHJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5001001
Product Code / EMDN: KHJ
Device Name: Preformed vocal cord medialization implant
Database Sync Date: 2026-08-09 09:08:30

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 Titanium-Vocal-Fold-Medial-Implant?

The registered manufacturer of record for Titanium-Vocal-Fold-Medial-Implant is Heinz Kurz GmbH.

What is the Primary UDI-DI identifier for Titanium-Vocal-Fold-Medial-Implant?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5001001.

What classification code is assigned to this device?

This device is registered under product classification code KHJ.

Similar Classification Devices (KHJ)

Other Devices by Heinz Kurz GmbH

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