Abbott clinical biochemical immunoglobulin A test group - Taiwan Registration 5e0697e5fc03cb491386bb16af810d52
Access comprehensive regulatory information for Abbott clinical biochemical immunoglobulin A 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 5e0697e5fc03cb491386bb16af810d52 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 Made (้จๅ่ฃฝ็จ) in JAPAN;; 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
5e0697e5fc03cb491386bb16af810d52
DHA00601782204
Product Details
Immunoglobulin A can be quantitatively analyzed in human serum or plasma.
C Immunology and microbiology
C.5510 ๅ ็ซ็่็ฝA,G,M,DๅEๅ ็ซ่ฉฆ้ฉ็ณป็ตฑ
Contract manufacturing;; input
Dates and Status
Dec 05, 2006
Dec 05, 2026

