Abbott urine/cerebrospinal fluid protein correction group - Taiwan Registration 2ba597d15b1e5f7d220599ebb21561db
Access comprehensive regulatory information for Abbott urine/cerebrospinal fluid protein correction group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ba597d15b1e5f7d220599ebb21561db 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.
Device Details
Registration Details
2ba597d15b1e5f7d220599ebb21561db
DHA05603214902
Product Details
Calibration of urine/cerebrospinal fluid protein test using Alinity c analyzer.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
Contract manufacturing;; input
Dates and Status
Jan 29, 2019
Jan 29, 2029

