Qui-visual chorionic gonadotropin assay reagent - Taiwan Registration d081393705c2943abd92683caa025eca
Access comprehensive regulatory information for Qui-visual chorionic gonadotropin assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d081393705c2943abd92683caa025eca and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIOMERIEUX CHINA LIMITED, TAIWAN BRANCH (HONG KONG).
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
Antibody antigen enzyme immune response to test human chorionic gonadotropin in serum or urine.
A Clinical chemistry and clinical toxicology
A.1155 Human chorionic gonadotropin testing system
import
Dates and Status
Oct 22, 2008
Oct 22, 2013
Aug 13, 2015
Cancellation Information
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