Api myoglobin test set calibration solution
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Mar 13, 2020 – Mar 13, 2030Active- Analysis ID
- 7040a8ad4568064cfa01bd318c82c9d3
- Customs Code
- DHA05603329100
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product is used to calibrate the Alinity i analyzer for the quantitative detection of myoglobin in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Mar 13, 2020
- Expiry Date
- Mar 13, 2030
Access comprehensive regulatory information for Api myoglobin test set calibration solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7040a8ad4568064cfa01bd318c82c9d3 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION. 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.