eudamed_udi Primary ID: 06975156256844

Marijuana (THC) Rapid Test (UDI 06975156256844)

Manufactured by Hangzhou Tongzhou Biotechnology Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Marijuana (THC) Rapid Test (Model/Catalog Number: D022-1001) is a medical device manufactured by Hangzhou Tongzhou Biotechnology 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: D022-1001
Product Code / EMDN: W0102160599
Device Name: Marijuana (THC) Rapid Test
Database Sync Date: 2026-08-09 16:46:39

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 Marijuana (THC) Rapid Test?

The registered manufacturer of record for Marijuana (THC) Rapid Test is Hangzhou Tongzhou Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for Marijuana (THC) Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975156256844.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Hangzhou Tongzhou Biotechnology Co., Ltd.

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