eudamed_udi Primary ID: 03597610626401

DENTASEPT SH PRO (UDI 03597610626401)

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 SH PRO (Model/Catalog Number: 2462326AO) 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: 2462326AO
Product Code / EMDN: D0901
Device Name: Dentasept SH pro
Database Sync Date: 2026-08-09 19:07:21

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 SH PRO?

The registered manufacturer of record for DENTASEPT SH PRO is D.M.D..

What is the Primary UDI-DI identifier for DENTASEPT SH PRO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610626401.

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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