Taiwan FDA registration 410c4c23ed7ecf141b59fd420e3cc4c5
"Artron" Helicobacter pylori (HP) Antigen Rapid Test (Non-Sterile)
TW: "艾創" 幽門桿菌抗原快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Mar 31, 2015 – Mar 31, 2020CancelledRegistration details
- Analysis ID
- 410c4c23ed7ecf141b59fd420e3cc4c5
- License Form
- Ministry of Health Medical Device Import No. 015061
- Customs Code
- DHA09401506101
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)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 31, 2015
- Expiry Date
- Mar 31, 2020
- Cancellation Date
- Sep 27, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Artron" Helicobacter pylori (HP) Antigen Rapid Test (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 410c4c23ed7ecf141b59fd420e3cc4c5 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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