Abbott second-generation urea nitrogen assay set - Taiwan Registration f4f482011ff4c68131d99bcaf0c4649d
Access comprehensive regulatory information for Abbott second-generation 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 f4f482011ff4c68131d99bcaf0c4649d and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. 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
Product Details
This product is used to quantify urea nitrogen in human serum, plasma or urine on the Alinity c System.
A Clinical chemistry and clinical toxicology
A.1770 ๅฐฟ็ด ๆฐฎ่ฉฆ้ฉ็ณป็ตฑ
Input;; QMS/QSD
Dates and Status
Dec 13, 2021
Dec 13, 2026

