Taiwan FDA registration 3df1b5c6920316e331c5df2aebc8d408

Longteng methylene dioxymethamphetamine (ecstasy) in vitro reagent group

TW: 龍騰亞甲基雙氧甲基安非他命(搖頭丸)體外試劑組
Taiwan flagTaiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Sep 09, 2008 – Sep 09, 2018Cancelled
Registration details
Analysis ID
3df1b5c6920316e331c5df2aebc8d408
Customs Code
DHY00500259803
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Qualitative detection of methylenedioxymethamphetamine (head shake pills) and its substitute products in human urine.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.3610 Methamphetamine testing system
Import Information
Domestic
Dates and status
Registration Date
Sep 09, 2008
Expiry Date
Sep 09, 2018
Cancellation Date
Jun 27, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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 3df1b5c6920316e331c5df2aebc8d408 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is The first factory of Longteng Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Longteng Biotechnology Co., Ltd. new market factory, 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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