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"Fujishi" Influenza virus type A and B rapid test reagent - Taiwan Registration 50aa761bdc934af669016b4cb7ff3470

Access comprehensive regulatory information for "Fujishi" Influenza virus type A and B 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 50aa761bdc934af669016b4cb7ff3470 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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50aa761bdc934af669016b4cb7ff3470
Registration Details
Taiwan FDA Registration: 50aa761bdc934af669016b4cb7ff3470
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Device Details

"Fujishi" Influenza virus type A and B rapid test reagent
TW: โ€œ่—คๅธโ€ ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹่ˆ‡Bๅž‹ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 2

Registration Details

50aa761bdc934af669016b4cb7ff3470

DHA05603369406

Product Details

This product can be used for the qualitative detection of Influenza virus (Flu) type A and B antigens in human nasopharyngeal swabs, nasopharyngeal irrigation solutions and throat swab samples.

C Immunology and microbiology

C.3328 Influenza Virus Antigen Rapid Screening and Detection System

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 26, 2020

Oct 26, 2025