Taiwan FDA registration 917583f23bfb38d1c0d638dad0a93e01
Kwai Ke Quick Know Pregnancy Test Pen
TW: 葵克快知 驗孕筆
Taiwan·Risk Class 2·PHAMATECH, INC·Registered May 16, 2008 – May 16, 2023ExpiredRegistration details
- Analysis ID
- 917583f23bfb38d1c0d638dad0a93e01
- Customs Code
- DHA00601904701
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 16, 2008
- Expiry Date
- May 16, 2023
About this record
Access comprehensive regulatory information for Kwai Ke Quick Know Pregnancy Test Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 917583f23bfb38d1c0d638dad0a93e01 and manufactured by PHAMATECH, INC. The authorized representative in Taiwan is GLOW STAR BIOTECH INC..
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