eudamed_udi Primary ID: 03597610626470

DENTASEPT ASPIRATION AF+ (UDI 03597610626470)

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 ASPIRATION AF+ (Model/Catalog Number: 2536137B6) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2536137B6
Product Code / EMDN: D99
Device Name: Dentasept Aspiration AF+
Database Sync Date: 2026-08-09 16:49:45

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 ASPIRATION AF+?

The registered manufacturer of record for DENTASEPT ASPIRATION AF+ is D.M.D..

What is the Primary UDI-DI identifier for DENTASEPT ASPIRATION AF+?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610626470.

What classification code is assigned to this device?

This device is registered under product classification code D99.

Similar Classification Devices (D99)

Other Devices by D.M.D.

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