Apex urea nitrogen assay set - Taiwan Registration 3657a12d46336747d55e3e2dfb204333
Access comprehensive regulatory information for Apex urea nitrogen assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3657a12d46336747d55e3e2dfb204333 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. 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
3657a12d46336747d55e3e2dfb204333
DHA05603199803
Product Details
This product can be used to quantify urea nitrogen in human serum, plasma or urine on the Alinity c analyzer.
A Clinical chemistry and clinical toxicology
A.1770 ๅฐฟ็ด ๆฐฎ่ฉฆ้ฉ็ณป็ตฑ
Contract manufacturing;; input
Dates and Status
Dec 28, 2018
Dec 28, 2028

