Taiwan FDA registration bb8d75330338752f679228efcec2b49d
"Yingfang" Helicobacter pylori antigen test kit (unsterilized)
TW: "瑩芳" 幽門螺旋桿菌抗原檢測試劑盒 (未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Jul 15, 2011 – Jul 15, 2026ExpiredRegistration details
- Analysis ID
- bb8d75330338752f679228efcec2b49d
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
- Domestic
Dates and status
- Registration Date
- Jul 15, 2011
- Expiry Date
- Jul 15, 2026
About this record
Access comprehensive regulatory information for "Yingfang" Helicobacter pylori antigen test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bb8d75330338752f679228efcec2b49d and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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