GUDIDData
eudamed_udi Primary ID: D-DMQL100Y8

Methaqualone Rapid Test (UDI D-DMQL100Y8)

Manufactured by Hangzhou Clongene Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Methaqualone Rapid Test - Primary ID D-DMQL100Y8

Device Regulatory Overview

The Methaqualone Rapid Test (Model/Catalog Number: DMQL1001 DMQL1002) is a medical device manufactured by Hangzhou Clongene Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DMQL1001 DMQL1002
Product Code / EMDN
W0102160599
Device Name
Methaqualone Rapid Test
Database Sync Date
2026-08-09 16:29:33

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Methaqualone Rapid Test?

The registered manufacturer of record for Methaqualone Rapid Test is Hangzhou Clongene Biotech Co., Ltd..

What is the Primary UDI-DI identifier for Methaqualone Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DMQL100Y8.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint