gudid Primary ID: 7007105,7007105-5,7007105-6

Dukal (UDI 7007105,7007105-5,7007105-6)

Manufactured by Dukal LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Dukal (Model/Catalog Number: 7007105,7007105-5,7007105-6) is a medical device manufactured by Dukal LLC. This product is indexed under FDA Product Code / Category Classification NAE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7007105,7007105-5,7007105-6
Product Code / EMDN: NAE
Device Name: Burn Gel Sachet
Database Sync Date: 2026-08-09 09:17:27

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 Dukal?

The registered manufacturer of record for Dukal is Dukal LLC.

What is the Primary UDI-DI identifier for Dukal?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7007105,7007105-5,7007105-6.

What classification code is assigned to this device?

This device is registered under product classification code NAE.

Similar Classification Devices (NAE)

Other Devices by Dukal LLC

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