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LZI THC (Cannabinoid) EIA Kit - Taiwan Registration 2984b4c17c9c168bc1f27d7039847aff

Access comprehensive regulatory information for LZI THC (Cannabinoid) EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2984b4c17c9c168bc1f27d7039847aff and manufactured by LIN-ZHI INTERNATIONAL, INC. The authorized representative in Taiwan is TAIWAN ADVANCE BIO-PHARMACEUTICAL INC..

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2984b4c17c9c168bc1f27d7039847aff
Registration Details
Taiwan FDA Registration: 2984b4c17c9c168bc1f27d7039847aff
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Device Details

LZI THC (Cannabinoid) EIA Kit
TW: ้ˆ่Šๅคง้บป้…ต็ด ๅ…็–ซ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

2984b4c17c9c168bc1f27d7039847aff

Ministry of Health Medical Device Import No. 031959

DHA05603195906

Company Information

United States

Product Details

The content of cannabis in human urine is determined qualitatively or semi-quantitatively, with a threshold of 50 ng/mL.

A Clinical chemistry and clinical toxicology

A3870 Cannabinoid Test System

Imported from abroad

Dates and Status

Dec 13, 2018

Dec 13, 2023