Taiwan FDA registration d198732595e7ef57703e14847d25ff35
Jieduo rapid pregnancy test reagent series
TW: 婕朵快速驗孕試劑系列
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Jan 18, 2012 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- d198732595e7ef57703e14847d25ff35
- Customs Code
- DHY00500350807
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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for Jieduo 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 d198732595e7ef57703e14847d25ff35 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is JIEDUO ENTERPRISE CO., LTD..
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