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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.

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3657a12d46336747d55e3e2dfb204333
Registration Details
Taiwan FDA Registration: 3657a12d46336747d55e3e2dfb204333
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Device Details

Apex urea nitrogen assay set
TW: ไบžๅŸนๅฐฟ็ด ๆฐฎๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

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 ๆฐฎ่ฉฆ้ฉ—็ณป็ตฑ

Contract manufacturing;; input

Dates and Status

Dec 28, 2018

Dec 28, 2028