gudid Primary ID: DEN6283

DawnMist (UDI DEN6283)

Manufactured by Dukal LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DawnMist (Model/Catalog Number: DEN6283) is a medical device manufactured by Dukal LLC. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DEN6283
Product Code / EMDN: EFT
Device Name: Denture Tablets
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 DawnMist?

The registered manufacturer of record for DawnMist is Dukal LLC.

What is the Primary UDI-DI identifier for DawnMist?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DEN6283.

What classification code is assigned to this device?

This device is registered under product classification code EFT.

Similar Classification Devices (EFT)

Other Devices by Dukal LLC

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