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Api creatinine assay set - Taiwan Registration c52045595ff92d2df7bd489bf8302220

Access comprehensive regulatory information for Api creatinine 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 c52045595ff92d2df7bd489bf8302220 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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c52045595ff92d2df7bd489bf8302220
Registration Details
Taiwan FDA Registration: c52045595ff92d2df7bd489bf8302220
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Device Details

Api creatinine assay set
TW: ไบžๅŸน่‚Œ้…ธ้…ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

c52045595ff92d2df7bd489bf8302220

DHA05603242401

Product Details

This product can be used to quantitatively determine creatinine in human serum, plasma or urine on the Alinity c analyzer.

A Clinical chemistry and clinical toxicology

A.1225 ่‚Œๆฐจ้…ธ้…่ฉฆ้ฉ—็ณป็ตฑ(Creatininetestsystem)

Input;; Contract manufacturing

Dates and Status

May 06, 2019

May 06, 2029