Taiwan FDA registration 25bc02a64b1a9768b2694f561e43dded
Kwai Ke Kuaizhi Ovulation Reagent (Unsterilized)
TW: 葵克快知 排卵試劑 (未滅菌)
Taiwan·Risk Class 1·PHAMATECH, INC·Registered Nov 16, 2009 – Nov 16, 2024ExpiredRegistration details
- Analysis ID
- 25bc02a64b1a9768b2694f561e43dded
- Customs Code
- DHA04400829806
Company information
- Manufacturer
- PHAMATECH, INC
- Manufacturer Country
- United States
- Authorized Representative
- GLOW STAR BIOTECH INC.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Luteinizing hormone test system (A.1485)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- import
Dates and status
- Registration Date
- Nov 16, 2009
- Expiry Date
- Nov 16, 2024
About this record
Access comprehensive regulatory information for Kwai Ke Kuaizhi Ovulation Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25bc02a64b1a9768b2694f561e43dded and manufactured by PHAMATECH, INC. The authorized representative in Taiwan is GLOW STAR BIOTECH INC..
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