Taiwan FDA registration 729f6aa2bbd84af7e4e750ba9a18e157
貝克曼庫爾特雌三醇試劑組(未滅菌)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Jul 17, 2024 – Jul 17, 2029ActiveRegistration details
- Analysis ID
- 729f6aa2bbd84af7e4e750ba9a18e157
- Customs Code
- DHA09402354605
Company information
- Manufacturer
- BECKMAN COULTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level of identification scope of the "Estriol Test System (A.1265)" of the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1265 雌三醇試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 17, 2024
- Expiry Date
- Jul 17, 2029
About this record
Access comprehensive regulatory information for 貝克曼庫爾特雌三醇試劑組(未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 729f6aa2bbd84af7e4e750ba9a18e157 and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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.
Free DatabasePowered by Pure Global AI89,000+ Devices