"Safety Assessment" Mycobacterium tuberculosis antibody rapid test reagent (unsterilized) - Taiwan Registration b420913495ca2ed5853dd931114e83f7
Access comprehensive regulatory information for "Safety Assessment" Mycobacterium tuberculosis 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 b420913495ca2ed5853dd931114e83f7 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..
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Device Details
Product Details
Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
C Immunology and microbiology
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import
Dates and Status
Dec 18, 2012
Dec 18, 2017
Jan 19, 2019
Cancellation Information
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