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LZI Amphetamines 500 EIA Kit - Taiwan Registration ccd4c02e21f43013cfc26de03ce61786

Access comprehensive regulatory information for LZI Amphetamines 500 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 ccd4c02e21f43013cfc26de03ce61786 and manufactured by LIN-ZHI INTERNATIONAL, INC. The authorized representative in Taiwan is TAIWAN ADVANCE BIO-PHARMACEUTICAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LIN-ZHI INTERNATIONAL, INC, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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ccd4c02e21f43013cfc26de03ce61786
Registration Details
Taiwan FDA Registration: ccd4c02e21f43013cfc26de03ce61786
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Device Details

LZI Amphetamines 500 EIA Kit
TW: ้ˆ่Šๅฎ‰้žไป–ๅ‘ฝ้…ต็ด ๅ…็–ซ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

ccd4c02e21f43013cfc26de03ce61786

Ministry of Health Medical Device Import No. 031423

DHA05603142304

Company Information

United States

Product Details

This product is used for the qualitative or semi-quantitative determination of amphetamines and methamphetamines in human urine and must be used with an automated biochemical analyzer with a threshold of 500ng/mL (corrected by d-methamphetamine).

A Clinical chemistry and clinical toxicology

A3100 Amphetamine Test System

Imported from abroad

Dates and Status

Aug 15, 2018

Aug 15, 2023

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