Taiwan FDA registration dab6fceb7f617c9d62f6a71a84882f43

"Mediflora" all-in-one substance abuse screening test kit

TW: “麥迪弗若拉” 多合一藥物濫用篩檢測試盒
Taiwan flagTaiwan·Risk Class 2·FIRSTEP BIORESEARCH INC.·Registered Dec 08, 2017 – Dec 23, 2019Cancelled
Registration details
Analysis ID
dab6fceb7f617c9d62f6a71a84882f43
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
FIRSTEP BIORESEARCH INC.
Product details
Intended Use
利用免疫定性分析法,檢驗人體尿液中之AMP, BAR, BZD, COC, MDMA, MET, MOR, PCP, THC, KET, MTD, BUP, PPX, TCA, K2, NMZ及其代謝物. 本產品可供專業人員及一般人士使用.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.3910 Tricyclic antidepressant test system;; A.3700 Prpasifene test system;; A.3610 Methamphetamine testing system
Import Information
Domestic
Dates and status
Registration Date
Dec 08, 2017
Expiry Date
Dec 23, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Mediflora" all-in-one substance abuse screening test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dab6fceb7f617c9d62f6a71a84882f43 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

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