Taiwan FDA registration b3a08de3a67727a188bddb53dbeaaf55

"Ichuang" rotavirus/adenovirus 2-in-1 rapid test (unsterilized)

TW: "艾創"輪狀病毒/腺病毒二合一快速檢測試劑(未滅菌)

Taiwan·Risk Class 1·ARTRON LABORATORIES INC.·Registered Feb 10, 2015 – Feb 10, 2020Cancelled

Registration details

Analysis ID: b3a08de3a67727a188bddb53dbeaaf55
Customs Code: DHA09401491002

Company information

Manufacturer: ARTRON LABORATORIES INC.
Manufacturer Country: Canada
Authorized Representative: YOULUM BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level of identification range of "polio virus serum reagent (C.3405)" and "adenovirus serum reagent (C.3020)" under the management measures for medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑;; C.3405 小兒麻痺病毒血清試劑
Import Information: import

Dates and status

Registration Date: Feb 10, 2015
Expiry Date: Feb 10, 2020
Cancellation Date: Sep 25, 2019

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Ichuang" rotavirus/adenovirus 2-in-1 rapid test (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3a08de3a67727a188bddb53dbeaaf55 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..

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