"Fujiji" human interstitial pneumonia virus rapid test reagent - Taiwan Registration 9ecbc993a3c4263baa25c487b714c803
Access comprehensive regulatory information for "Fujiji" human interstitial pneumonia virus rapid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ecbc993a3c4263baa25c487b714c803 and manufactured by TAUNS LABORATORIES, INC., KAMISHIMA FACTORY;; TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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Device Details
Product Details
This product can be used to detect the presence of human metapneumovirus antigens in nasal swabs, nasal irrigation fluids or throat swabs.
C Immunology and microbiology
C.9999 Miscellaneous
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Apr 11, 2022
Apr 11, 2027