Taiwan FDA registration eea0d807dc319a7942385b10bc6c99a2
"Artron" Adenovirus Test Kit (Non-sterile)
TW: "艾創"腺病毒快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Feb 10, 2015 – Feb 10, 2020CancelledRegistration details
- Analysis ID
- eea0d807dc319a7942385b10bc6c99a2
- License Form
- Ministry of Health Medical Device Import No. 014911
- Customs Code
- DHA09401491101
Company information
- Manufacturer
- ARTRON LABORATORIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- YOULUM BIOTECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
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 "Artron" Adenovirus Test Kit (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eea0d807dc319a7942385b10bc6c99a2 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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