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Abbott clinical biochemical immunoglobulin G test group - Taiwan Registration ea24d04ccb889bececb115668a3fc12e

Access comprehensive regulatory information for Abbott clinical biochemical immunoglobulin G test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea24d04ccb889bececb115668a3fc12e 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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ea24d04ccb889bececb115668a3fc12e
Registration Details
Taiwan FDA Registration: ea24d04ccb889bececb115668a3fc12e
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Device Details

Abbott clinical biochemical immunoglobulin G test group
TW: ไบžๅŸน่‡จๅบŠ็”ŸๅŒ–ๅ…็–ซ็ƒ่›‹็™ฝGๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

ea24d04ccb889bececb115668a3fc12e

DHA00601761308

Product Details

Immunoglobulin G in human serum or plasma can be quantitatively analyzed.

C Immunology and microbiology

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

Contract manufacturing;; input

Dates and Status

Nov 22, 2006

Nov 22, 2026

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