Pure Global

Abbott Designer Galliglutinin-3 Test Set - Taiwan Registration be5dafdbcdf42bb45388fe5b22b929fd

Access comprehensive regulatory information for Abbott Designer Galliglutinin-3 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 be5dafdbcdf42bb45388fe5b22b929fd and manufactured by FUJIREBIO DIAGNOSTICS, 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
be5dafdbcdf42bb45388fe5b22b929fd
Registration Details
Taiwan FDA Registration: be5dafdbcdf42bb45388fe5b22b929fd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Abbott Designer Galliglutinin-3 Test Set
TW: ไบžๅŸน่จญ่จˆๅธซๅŠไนณ้†ฃๅ‡้›†็ด -3ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

be5dafdbcdf42bb45388fe5b22b929fd

DHA05603203704

Company Information

Product Details

This product is a chemical cold light particle immunoassay (CMIA) used in conjunction with the ARCHITECT i system for the quantitative detection of galactoglutinin-3 (galectin-3) in human serum and EDTA plasma. The efficacy (discretionary) was changed to: This product was used to quantitatively detect galactoglutinin-3 (galectin-3) in human serum and EDTA plasma by chemical cold light particle immunoassay (CMIA).

A Clinical chemistry and clinical toxicology

A.1660 Grade Material (Analysis Material Non-Analysis);; A.1117 Type B diuretic ้ˆ‰่‚ฝ่ฉฆ้ฉ—็ณป็ตฑ;; A.1150 Calibrated Products

Contract manufacturing;; input

Dates and Status

Jan 14, 2019

Jan 14, 2029