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Mei Ariel Ji Yazi Eight Drug Abuse Test Kits - Taiwan Registration 5b5868963c0d35fe1e39970ef86aabf8

Access comprehensive regulatory information for Mei Ariel Ji Yazi Eight Drug Abuse Test Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b5868963c0d35fe1e39970ef86aabf8 and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

This page provides complete technical specifications, regulatory compliance details. 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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5b5868963c0d35fe1e39970ef86aabf8
Registration Details
Taiwan FDA Registration: 5b5868963c0d35fe1e39970ef86aabf8
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Device Details

Mei Ariel Ji Yazi Eight Drug Abuse Test Kits
TW: ็พŽ่‰พๅˆฉ็ˆพ ๆฃ่€ถๆฟŸ ๅ…ซ้กž่—ฅ็‰ฉๆฟซ็”จๆชขๆธฌๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

5b5868963c0d35fe1e39970ef86aabf8

DHA00601617900

Company Information

United States

Product Details

Urine is qualitatively detected for amphetamines, barbiturates, benzodiazepines, cocaine, methadone, opium, tetrahydrocanabinol and their metabolites, and the presence of tricyclic antidepressants at specific cut-off values.

A Clinical chemistry and clinical toxicology

A.3100 Anandamide Test System

import

Dates and Status

Mar 21, 2006

Mar 21, 2021

Oct 12, 2023

Cancellation Information

Logged out

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