Taiwan FDA registration 47f342ea41a1488c7734d9a1e05d62e3
Kwai Ke Quick Know Pregnancy Test Tablets
TW: 葵克快知 驗孕片
Taiwan·Risk Class 2·PHAMATECH, INC·Registered May 28, 2008 – May 28, 2023ExpiredRegistration details
- Analysis ID
- 47f342ea41a1488c7734d9a1e05d62e3
- Customs Code
- DHA00601906207
Company information
- Manufacturer
- PHAMATECH, INC
- Manufacturer Country
- United States
- Authorized Representative
- GLOW STAR BIOTECH INC.
Product details
- Intended Use
- Detection of human chorionic gonadotropin hCG in urine as a test for early diagnosis of pregnancy.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- import
Dates and status
- Registration Date
- May 28, 2008
- Expiry Date
- May 28, 2023
About this record
Access comprehensive regulatory information for Kwai Ke Quick Know Pregnancy Test Tablets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47f342ea41a1488c7734d9a1e05d62e3 and manufactured by PHAMATECH, INC. The authorized representative in Taiwan is GLOW STAR BIOTECH INC..
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