Abbott clinical biochemical immunoglobulin M assay group - Taiwan Registration f3ff78f306bebe378004fb25591860e2
Access comprehensive regulatory information for Abbott clinical biochemical immunoglobulin M assay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3ff78f306bebe378004fb25591860e2 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, 1 companies making similar products including ABBOTT IRELAND DIAGNOSTICS DIVISION, 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
Registration Details
f3ff78f306bebe378004fb25591860e2
DHA00601782701
Product Details
The content of Immunoglobulin M in human serum or plasma can be quantified.
C Immunology and microbiology
C.5510 ๅ ็ซ็่็ฝA,G,M,DๅEๅ ็ซ่ฉฆ้ฉ็ณป็ตฑ
Contract manufacturing;; input
Dates and Status
Dec 13, 2006
Dec 13, 2026

