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Apex complement C3 assay group - Taiwan Registration a403dd3e56d56a19a5a489ba42af67ae

Access comprehensive regulatory information for Apex complement C3 assay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a403dd3e56d56a19a5a489ba42af67ae 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, 1 companies making similar products including Made (้ƒจๅˆ†่ฃฝ็จ‹) in JAPAN;; ABBOTT IRELAND DIAGNOSTICS DIVISION, and 1 recent registrations in the same category. 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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a403dd3e56d56a19a5a489ba42af67ae
Registration Details
Taiwan FDA Registration: a403dd3e56d56a19a5a489ba42af67ae
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Device Details

Apex complement C3 assay group
TW: ไบžๅŸน่ฃœ้ซ”C3ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

a403dd3e56d56a19a5a489ba42af67ae

DHA05603217302

Product Details

This product quantifies Complement C3 in human serum or plasma on an Alinity c analyzer.

C Immunology and microbiology

C.5240 ่ฃœ้ซ”ๆˆไปฝๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Feb 13, 2019

Feb 13, 2029

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