Taiwan FDA registration 17fe970e383d1e4b7e33bd7927e3b83f
Sunflower rapid pregnancy test reagent series
TW: 向日葵快速驗孕試劑系列
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Feb 21, 2012 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- 17fe970e383d1e4b7e33bd7927e3b83f
- Customs Code
- DHY00500359107
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HAN CHUAN MEDICAL MATERIAL BIO-TEC CO., LTD.
Product details
- Intended Use
- Serum or urine is tested for human chorionic gonadotropin (HCG). 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
- Feb 21, 2012
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for Sunflower 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 17fe970e383d1e4b7e33bd7927e3b83f and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is HAN CHUAN MEDICAL MATERIAL BIO-TEC CO., LTD..
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