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Longteng methylene dioxymethamphetamine (ecstasy) in vitro reagent group - Taiwan Registration 8acbd230e0707defdb5e1fd75008c200

Access comprehensive regulatory information for Longteng methylene dioxymethamphetamine (ecstasy) in vitro reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8acbd230e0707defdb5e1fd75008c200 and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is Longteng Biotechnology Co., Ltd. new market factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including The first factory of Longteng Biotechnology Co., Ltd, 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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8acbd230e0707defdb5e1fd75008c200
Registration Details
Taiwan FDA Registration: 8acbd230e0707defdb5e1fd75008c200
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Device Details

Longteng methylene dioxymethamphetamine (ecstasy) in vitro reagent group
TW: ้พ้จฐไบž็”ฒๅŸบ้›™ๆฐง็”ฒๅŸบๅฎ‰้žไป–ๅ‘ฝ(ๆ–้ ญไธธ)้ซ”ๅค–่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

8acbd230e0707defdb5e1fd75008c200

Company Information

Product Details

Qualitative detection of methylenedioxymethamphetamine (ecstasy) and its metabolites in human urine.

A Clinical chemistry and clinical toxicology

A.3610 Methamphetamine testing system

Domestic

Dates and Status

Feb 24, 2020

Feb 24, 2030

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