Fukushima Kotake pylori rapid assay reagent - Taiwan Registration 514611e2825f4e2747f742279809f6ed
Access comprehensive regulatory information for Fukushima Kotake pylori rapid assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 514611e2825f4e2747f742279809f6ed and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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.
Device Details
Product Details
Qualitative detection of Helicobacter pylori IgG antibodies in human whole blood, plasma, and serum.
C Immunology and microbiology
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import
Dates and Status
Dec 22, 2005
Dec 22, 2010
Nov 20, 2012
Cancellation Information
Logged out
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