Apex immunoglobulin G test set - Taiwan Registration d358f94f61289b65e376dbdd329bda6f
Access comprehensive regulatory information for Apex immunoglobulin G test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d358f94f61289b65e376dbdd329bda6f 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
d358f94f61289b65e376dbdd329bda6f
DHA05603238004
Product Details
This product quantitatively determines immunoglobulin G in human serum or plasma on the Alinity c analyzer.
C Immunology and microbiology
C.5510 ๅ ็ซ็่็ฝA,G,M,DๅEๅ ็ซ่ฉฆ้ฉ็ณป็ตฑ
Input;; Contract manufacturing
Dates and Status
Mar 25, 2019
Mar 25, 2029

