Api creatinine assay set
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered May 06, 2019 – May 06, 2029Active- Analysis ID
- c52045595ff92d2df7bd489bf8302220
- Customs Code
- DHA05603242401
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product can be used to quantitatively determine creatinine in human serum, plasma or urine on the Alinity c analyzer.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1225 肌氨酸酐試驗系統(Creatininetestsystem)
- Import Information
- Input;; Contract manufacturing
- Registration Date
- May 06, 2019
- Expiry Date
- May 06, 2029
Access comprehensive regulatory information for Api creatinine assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c52045595ff92d2df7bd489bf8302220 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC 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.