Taiwan FDA registration 75ea998c3b06a9cfa76e2a035021a4dc
Firstep Synthetic cannabis (K2) Drug Screen Test
TW: 聯華合成大麻(辣大麻)藥物濫用篩檢測試組
Registration details
- Analysis ID
- 75ea998c3b06a9cfa76e2a035021a4dc
- License Form
- Ministry of Health Medical Device Manufacturing No. 005368
Company information
- Manufacturer
- FIRSTEP BIORESEARCH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FIRSTEP BIORESEARCH INC.
Product details
- Intended Use
- Synthetic cannabis, K2, JWH-073 metabolites in urine were detected by immunoqualitative analysis, and the results were interpreted by naked eye to preliminarily screen for drug abuse of synthetic marijuana. This product can be used by professionals and the general public. The detection thresholds of this product are JWH-018 50 ng/mL and JWH-073 25 ng/mL. This product is used as a preliminary screening for the abuse of synthetic cannabis drugs, if drug abuse is suspected, a gas chromatography mass spectrometry (GC/MS) test is required for confirmatory test.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A3870 Cannabinoid Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 18, 2017
- Expiry Date
- Jan 18, 2027
About this record
Access comprehensive regulatory information for Firstep Synthetic cannabis (K2) Drug Screen Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75ea998c3b06a9cfa76e2a035021a4dc and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..
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