eudamed_udi Primary ID: 03597610488702

QUITANET ULTRA (UDI 03597610488702)

Manufactured by D.M.D.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The QUITANET ULTRA (Model/Catalog Number: 2762092L6) 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: 2762092L6
Product Code / EMDN: D0901
Device Name: QUITANET ULTRA 12X1L
Database Sync Date: 2026-08-09 18:19:38

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 QUITANET ULTRA?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610488702.

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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