"Fujiji" human interstitial pneumonia virus rapid test reagent
Taiwan·Risk Class 2·TAUNS LABORATORIES, INC., KAMISHIMA FACTORY;; TAUNS LABORATORIES, INC.·Registered Apr 11, 2022 – Apr 11, 2027Active- Analysis ID
- 9ecbc993a3c4263baa25c487b714c803
- Customs Code
- DHA05603523602
- Manufacturer Country
- Japan
- Authorized Representative
- YOULUM BIOTECHNOLOGY CO., LTD.
- Intended Use
- This product can be used to detect the presence of human metapneumovirus antigens in nasal swabs, nasal irrigation fluids or throat swabs.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.9999 Miscellaneous
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Apr 11, 2022
- Expiry Date
- Apr 11, 2027
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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