eudamed_udi Primary ID: D-69384449MDMA01TQ

DAVID (UDI D-69384449MDMA01TQ)

Manufactured by Equinox Biotech Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DAVID (Model/Catalog Number: RH-MDMA-S, RH-MDMA-C) is a medical device manufactured by Equinox 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: RH-MDMA-S, RH-MDMA-C
Product Code / EMDN: W0102160599
Device Name: One Step MDMA Screen Test (Urine)
Database Sync Date: 2026-08-09 16:28:46

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 DAVID?

The registered manufacturer of record for DAVID is Equinox Biotech Co., Ltd..

What is the Primary UDI-DI identifier for DAVID?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-69384449MDMA01TQ.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Equinox Biotech Co., Ltd.

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