Taiwan FDA registration 38aaba740fa06584fe3376338f82fbf7
Alpha Pregnancy Rapid Test Reagent
TW: 阿爾發懷孕快速檢測試劑
Taiwan·Risk Class 2·ALFA SCIENTIFIC DESIGNS, INC.·Registered Feb 27, 2006 – Feb 27, 2026ExpiredRegistration details
- Analysis ID
- 38aaba740fa06584fe3376338f82fbf7
- Customs Code
- DHA00601605600
Company information
- Manufacturer
- ALFA SCIENTIFIC DESIGNS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- The Urine Pregnancy Rapid Test is a rapid, qualitative, single-step test for the measurement of chorionic gonadotropin (HCG) in human urine or serum as a diagnosis of early 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
- Feb 27, 2006
- Expiry Date
- Feb 27, 2026
About this record
Access comprehensive regulatory information for Alpha Pregnancy Rapid Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38aaba740fa06584fe3376338f82fbf7 and manufactured by ALFA SCIENTIFIC DESIGNS, INC.. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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