eudamed_udi Primary ID: 03597610639173

DENTASEPT ULTRA (UDI 03597610639173)

Manufactured by D.M.D.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DENTASEPT ULTRA (Model/Catalog Number: 293034GC) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D01010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 293034GC
Product Code / EMDN: D01010102
Device Name: Dentasept Ultra 4x5L
Database Sync Date: 2026-08-09 17:29:43

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 DENTASEPT ULTRA?

The registered manufacturer of record for DENTASEPT ULTRA is D.M.D..

What is the Primary UDI-DI identifier for DENTASEPT ULTRA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610639173.

What classification code is assigned to this device?

This device is registered under product classification code D01010102.

Similar Classification Devices (D01010102)

Other Devices by D.M.D.

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