Taiwan FDA registration ea24d04ccb889bececb115668a3fc12e

Abbott clinical biochemical immunoglobulin G test group

TW: 亞培臨床生化免疫球蛋白G檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Nov 22, 2006 – Nov 22, 2026Active
Registration details
Analysis ID
ea24d04ccb889bececb115668a3fc12e
Customs Code
DHA00601761308
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
Immunoglobulin G in human serum or plasma can be quantitatively analyzed.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Nov 22, 2006
Expiry Date
Nov 22, 2026
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About this record

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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