Taiwan FDA registration 1d9b397d64c595ce53943bac465b63a8
"Artron" Rotavirus Test Kit (Non-Sterile)
TW: "艾創"輪狀病毒快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Feb 10, 2015 – Feb 10, 2020CancelledRegistration details
- Analysis ID
- 1d9b397d64c595ce53943bac465b63a8
- License Form
- Ministry of Health Medical Device Import No. 014912
- Customs Code
- DHA09401491203
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)
- C3405 Polio virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 10, 2015
- Expiry Date
- Feb 10, 2020
- Cancellation Date
- Oct 02, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Artron" Rotavirus 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 1d9b397d64c595ce53943bac465b63a8 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices