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LZI Amphetamines 500 EIA Kit - Taiwan Registration 14980f460b2117d055c8c9dffedcdf36

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 14980f460b2117d055c8c9dffedcdf36 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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14980f460b2117d055c8c9dffedcdf36
Registration Details
Taiwan FDA Registration: 14980f460b2117d055c8c9dffedcdf36
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Device Details

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

Registration Details

14980f460b2117d055c8c9dffedcdf36

Ministry of Health Medical Device Import No. 031803

DHA05603180301

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 needs to 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

Nov 21, 2018

Nov 21, 2028

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