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Apex immunoglobulin G test set - Taiwan Registration d358f94f61289b65e376dbdd329bda6f

Access comprehensive regulatory information for Apex immunoglobulin G test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d358f94f61289b65e376dbdd329bda6f 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 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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d358f94f61289b65e376dbdd329bda6f
Registration Details
Taiwan FDA Registration: d358f94f61289b65e376dbdd329bda6f
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Device Details

Apex immunoglobulin G test set
TW: ไบžๅŸนๅ…็–ซ็ƒ่›‹็™ฝGๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

d358f94f61289b65e376dbdd329bda6f

DHA05603238004

Product Details

This product quantitatively determines immunoglobulin G in human serum or plasma on the Alinity c analyzer.

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Mar 25, 2019

Mar 25, 2029

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