Taiwan FDA registration 50aa761bdc934af669016b4cb7ff3470

"Fujishi" Influenza virus type A and B rapid test reagent

TW: “藤司” 流行性感冒病毒A型與B型快速檢測試劑

Taiwan·Risk Class 2·TAUNS LABORATORIES, INC., KAMISHIMA FACTORY;; TAUNS LABORATORIES, INC.·Registered Oct 26, 2020 – Oct 26, 2025Expired

Registration details

Analysis ID: 50aa761bdc934af669016b4cb7ff3470
Customs Code: DHA05603369406

Company information

Manufacturer: TAUNS LABORATORIES, INC., KAMISHIMA FACTORY;; TAUNS LABORATORIES, INC.
Manufacturer Country: Japan
Authorized Representative: YOULUM BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3328 Influenza Virus Antigen Rapid Screening and Detection System
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Oct 26, 2020
Expiry Date: Oct 26, 2025

About this record

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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