eudamed_udi Primary ID: 03597610629785

DENTASEPT SPECIAL ROTATIVE (UDI 03597610629785)

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 SPECIAL ROTATIVE (Model/Catalog Number: 2480047DA) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2480047DA
Product Code / EMDN: D0901
Device Name: DENTASEPT SPECIAL ROTATIVE 1X5L
Database Sync Date: 2026-08-09 18:21:43

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 SPECIAL ROTATIVE?

The registered manufacturer of record for DENTASEPT SPECIAL ROTATIVE is D.M.D..

What is the Primary UDI-DI identifier for DENTASEPT SPECIAL ROTATIVE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610629785.

What classification code is assigned to this device?

This device is registered under product classification code D0901.

Similar Classification Devices (D0901)

Other Devices by D.M.D.

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