Taiwan FDA registration 6d6c7fa9ae4f0aea0941ec7e44becfbd
Dongyao Kaitamine/Ecstasy double test rapid test reagent
TW: 東耀愷他命/搖頭丸雙測快速檢驗試劑
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Jul 06, 2015 – Jul 06, 2025ExpiredRegistration details
- Analysis ID
- 6d6c7fa9ae4f0aea0941ec7e44becfbd
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TONYAR BIOTECH. INC.
Product details
- Intended Use
- Competitive immunochromatography was used to qualitatively detect whether human urine contained Ketamine, KET, K and MDMA.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3610 Methamphetamine testing system;; A.0001 Phencyclidine test system
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 06, 2015
- Expiry Date
- Jul 06, 2025
About this record
Access comprehensive regulatory information for Dongyao Kaitamine/Ecstasy double test rapid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d6c7fa9ae4f0aea0941ec7e44becfbd and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TONYAR BIOTECH. INC..
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