Apex complement C3 assay group - Taiwan Registration a403dd3e56d56a19a5a489ba42af67ae
Access comprehensive regulatory information for Apex complement C3 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 a403dd3e56d56a19a5a489ba42af67ae 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
a403dd3e56d56a19a5a489ba42af67ae
DHA05603217302
Product Details
This product quantifies Complement C3 in human serum or plasma on an Alinity c analyzer.
C Immunology and microbiology
C.5240 ่ฃ้ซๆไปฝๅ ็ซ่ฉฆ้ฉ็ณป็ตฑ
Input;; Contract manufacturing
Dates and Status
Feb 13, 2019
Feb 13, 2029

