Abbott microalbumin test reagent group quality control solution and correction solution
- Analysis ID
- bc0f559a7528318168e4686846fb274f
- Customs Code
- DHA05603216806
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- It is used for the correction of Alinity c microalbumin test on the Alinity c analyzer.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical); A.1150 calibration
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Feb 13, 2019
- Expiry Date
- Feb 13, 2029
Access comprehensive regulatory information for Abbott microalbumin test reagent group quality control solution and correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc0f559a7528318168e4686846fb274f 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.