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
Registration details
- Analysis ID
- dab6fceb7f617c9d62f6a71a84882f43
Company information
- Manufacturer
- FIRSTEP BIORESEARCH INC.
- 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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