Taiwan FDA registration 896e0397ca36abfd58acc6196e37986e
"Avi" Rotavirus/Adenovirus Rapid Test Reagent (Unsterilized)
TW: “愛威” 輪狀病毒/腺病毒快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·AVE SCIENCE & TECHNOLOGY CO., LTD.·Registered Aug 13, 2020 – Aug 13, 2025ExpiredRegistration details
- Analysis ID
- 896e0397ca36abfd58acc6196e37986e
- Customs Code
- DHA09600428601
Company information
- Manufacturer
- AVE SCIENCE & TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- DiaTech Technology Co., Ltd.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" and "Poliovirus Serum Reagent (C.3405)" of the Classification and Grading 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
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 13, 2020
- Expiry Date
- Aug 13, 2025
About this record
Access comprehensive regulatory information for "Avi" Rotavirus/Adenovirus Rapid 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 896e0397ca36abfd58acc6196e37986e and manufactured by AVE SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
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