Taiwan FDA registration 518b41b76e93610b1e4ced6bb44aa7d4
Kwai Que Creek Follicle-stimulating Reagent (Unsterilized)
TW: 葵克快知 卵泡刺激素試劑 (未滅菌)
Registration details
- Analysis ID
- 518b41b76e93610b1e4ced6bb44aa7d4
- Customs Code
- DHA04400847706
Company information
- Manufacturer
- PHAMATECH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GLOW STAR BIOTECH INC.
Product details
- Intended Use
- It is limited to the first level of identification of the follicular stimulation hormone test system (A.1300) of the classification and grading management method of medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1300 Follicular Stimulation Hormone Test System
- Import Information
- import
Dates and status
- Registration Date
- Jan 20, 2010
- Expiry Date
- Jan 20, 2025
About this record
Access comprehensive regulatory information for Kwai Que Creek Follicle-stimulating 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 518b41b76e93610b1e4ced6bb44aa7d4 and manufactured by PHAMATECH, INC.. The authorized representative in Taiwan is GLOW STAR BIOTECH INC..
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