"Dibo" Kabili Mycobacterium tuberculosis antigen rapid identification reagent (unsterilized) - Taiwan Registration 5057891ca1e8583576bcb794530d6849
Access comprehensive regulatory information for "Dibo" Kabili Mycobacterium tuberculosis antigen rapid identification 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 5057891ca1e8583576bcb794530d6849 and manufactured by TAUNS LABORATORIES, INC. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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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
Feb 25, 2013
Feb 25, 2018
Mar 20, 2013
Cancellation Information
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