Taiwan FDA registration a6e280fc8dc6f162749bc1fe0a6683ea
Kwai Ke Quick Know Pregnancy Test Plate
TW: 葵克快知 驗孕盤
Taiwan·Risk Class 2·PHAMATECH, INC·Registered Jun 10, 2008 – Jun 10, 2023ExpiredRegistration details
- Analysis ID
- a6e280fc8dc6f162749bc1fe0a6683ea
- Customs Code
- DHA00601908200
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
- Jun 10, 2008
- Expiry Date
- Jun 10, 2023
About this record
Access comprehensive regulatory information for Kwai Ke Quick Know Pregnancy Test Plate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a6e280fc8dc6f162749bc1fe0a6683ea and manufactured by PHAMATECH, INC. The authorized representative in Taiwan is GLOW STAR BIOTECH INC..
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