eudamed_udi Primary ID: D-DCOC100RH

Cocaine Rapid Test (UDI D-DCOC100RH)

Manufactured by Hangzhou Clongene Biotech Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cocaine Rapid Test (Model/Catalog Number: DCOC1001, DCOC1002, DCOC1004) is a medical device manufactured by Hangzhou Clongene Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160506 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DCOC1001, DCOC1002, DCOC1004
Product Code / EMDN: W0102160506
Device Name: Cocaine Rapid Test
Database Sync Date: 2026-08-09 18:25:30

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 Cocaine Rapid Test?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DCOC100RH.

What classification code is assigned to this device?

This device is registered under product classification code W0102160506.

Similar Classification Devices (W0102160506)

Other Devices by Hangzhou Clongene Biotech Co., Ltd.

Programmatic Export

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

JSON API Endpoint