Taiwan FDA registration 52cd036b596f37c9f4c1792dc63d8d3e
"Drairy" rapid pregnancy test reagent series
TW: “德萊莉” 快速驗孕試劑系列
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Jul 08, 2015 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- 52cd036b596f37c9f4c1792dc63d8d3e
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JIEDUO ENTERPRISE CO., LTD.
Product details
- Intended Use
- The change in efficacy (removal of serum source and addition of non-specialist use) is the qualitative test of urine for human chorionic gonadotropin (HCG).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jul 08, 2015
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for "Drairy" rapid pregnancy test reagent series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52cd036b596f37c9f4c1792dc63d8d3e and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is JIEDUO ENTERPRISE CO., LTD..
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