eudamed_udi Primary ID: 03597610488726

QUITANET ENZYME (UDI 03597610488726)

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 ENZYME (Model/Catalog Number: 2759092) 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: 2759092
Product Code / EMDN: D0901
Device Name: QUITANET ENZYME 12X1L
Database Sync Date: 2026-08-09 18:15:49

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 ENZYME?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610488726.

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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