eudamed_udi Primary ID: 03597610627163

Dentasept Spray 60 Pro (UDI 03597610627163)

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 Spray 60 Pro (Model/Catalog Number: 24755009Z) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 24755009Z
Product Code / EMDN: D0701
Device Name: Dentasept Spray 60 Pro 3x1L
Database Sync Date: 2026-08-09 18:33:43

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 Spray 60 Pro?

The registered manufacturer of record for Dentasept Spray 60 Pro is D.M.D..

What is the Primary UDI-DI identifier for Dentasept Spray 60 Pro?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610627163.

What classification code is assigned to this device?

This device is registered under product classification code D0701.

Similar Classification Devices (D0701)

Other Devices by D.M.D.

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