Taiwan FDA registration 9253f190dd79fd85eaa0f86bd6e8c5f6
"Yingfang" Aspergillus pylori urease rapid test strip (unsterilized)
TW: "瑩芳" 幽門曲狀桿菌尿素酶快速檢測試紙(未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Apr 14, 2023 – Apr 14, 2028ActiveRegistration details
- Analysis ID
- 9253f190dd79fd85eaa0f86bd6e8c5f6
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG 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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Apr 14, 2023
- Expiry Date
- Apr 14, 2028
About this record
Access comprehensive regulatory information for "Yingfang" Aspergillus pylori urease rapid test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9253f190dd79fd85eaa0f86bd6e8c5f6 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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