Taiwan FDA registration ca0d1c07fec57522de7ff83c2aaa8bdf
"Yingfang" Helicobacter pylori rapid test reagent (unsterilized)
TW: "瑩芳" 幽門螺旋桿菌快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Jul 15, 2011 – Jul 15, 2026ExpiredRegistration details
- Analysis ID
- ca0d1c07fec57522de7ff83c2aaa8bdf
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 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 ca0d1c07fec57522de7ff83c2aaa8bdf and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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