Abbott clinical biochemical immunoglobulin G test group - Taiwan Registration 773e10b461c0c85b767852023afb0e7e
Access comprehensive regulatory information for Abbott clinical biochemical immunoglobulin G test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 773e10b461c0c85b767852023afb0e7e and manufactured by 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, 1 companies making similar products including FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH, and 1 recent registrations in the same category. 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
Product Details
This product is used to quantify IgG in human serum or plasma on the ARCHITECT c system.
C Immunology and microbiology
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Dates and Status
Jan 25, 2022
Jan 25, 2027

