Taiwan FDA registration 5257d8bbcb1cf3cfb5efa8c4f7d135a0
"Aiwe" Helicobacter pylori rapid test reagent (unsterilized)
TW: “愛威” 幽門螺旋桿菌快速檢測試劑(未滅菌)
Registration details
- Analysis ID
- 5257d8bbcb1cf3cfb5efa8c4f7d135a0
- Customs Code
- DHA09600430202
Company information
- Manufacturer
- AVE SCIENCE & TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- DiaTech Technology Co., Ltd.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 31, 2020
- Expiry Date
- Aug 31, 2025
About this record
Access comprehensive regulatory information for "Aiwe" Helicobacter pylori 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 5257d8bbcb1cf3cfb5efa8c4f7d135a0 and manufactured by AVE SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
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