Taiwan FDA registration 813f87d2684385c441b84d69d82fdc32
ASK Ketamine Rapid Test
TW: 東耀愷他命快速檢驗試劑
Taiwan·Risk Class 2·MD·TONYAR BIOTECH. INC.·Registered Aug 06, 2014 – Aug 06, 2024ExpiredRegistration details
- Analysis ID
- 813f87d2684385c441b84d69d82fdc32
- License Form
- Ministry of Health Medical Device Manufacturing No. 004704
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TONYAR BIOTECH. INC.
Product details
- Intended Use
- Competitive immunochromatography to qualitatively detect the presence of katamine in human urine (Ketamine, KET, Ktamine, ketamine)
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A0001 Phencyclidine Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 06, 2014
- Expiry Date
- Aug 06, 2024
About this record
Access comprehensive regulatory information for ASK Ketamine Rapid Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 813f87d2684385c441b84d69d82fdc32 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TONYAR BIOTECH. INC..
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