Taiwan FDA registration 8af9e656fd40b732aff5fe9023b60cf1

"Fujishi" type A streptococcus test reagent (unsterilized)

TW: “藤司”A型鏈球菌檢驗試劑(未滅菌)

Taiwan·Risk Class 1·TAUNS LABORATORIES, INC., KAMISHIMA FACTORY;; TAUNS LABORATORIES, INC.·Registered Mar 15, 2022 – Mar 15, 2027Active

Registration details

Analysis ID: 8af9e656fd40b732aff5fe9023b60cf1
Customs Code: DHA09402276002

Company information

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

Product details

Intended Use: Classification and grading management method of medical equipment: Streptococcus belongs to the first level identification range of serum reagent (C.3740).
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3740 鏈球菌屬血清試劑
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Mar 15, 2022
Expiry Date: Mar 15, 2027

About this record

Access comprehensive regulatory information for "Fujishi" type A streptococcus test 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 8af9e656fd40b732aff5fe9023b60cf1 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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