"Safety Assessment" Pylori Antibody Rapid Test Reagent (Unsterilized) - Taiwan Registration 8d0493b6c05b4fefef42750e433e47d3
Access comprehensive regulatory information for "Safety Assessment" Pylori Antibody Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d0493b6c05b4fefef42750e433e47d3 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is JOLEX INTERNATIONAL 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
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
C Immunology and microbiology
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import
Dates and Status
Dec 18, 2012
Dec 18, 2017
Jan 17, 2019
Cancellation Information
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