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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.

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f4f482011ff4c68131d99bcaf0c4649d
Registration Details
Taiwan FDA Registration: f4f482011ff4c68131d99bcaf0c4649d
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Device Details

Abbott second-generation urea nitrogen assay set
TW: ไบžๅŸน็ฌฌไบŒไปฃๅฐฟ็ด ๆฐฎๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

f4f482011ff4c68131d99bcaf0c4649d

DHA05603492109

Company Information

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 ๆฐฎ่ฉฆ้ฉ—็ณป็ตฑ

Input;; QMS/QSD

Dates and Status

Dec 13, 2021

Dec 13, 2026