Taiwan FDA registration 8c46841b4d9176661156582b2548d244
Yingfang Rapid Test Reagent for Influenza A/B (Unsterilized)
TW: "瑩芳" A/B 型流感快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Jul 31, 2015 – Jul 31, 2025ExpiredRegistration details
- Analysis ID
- 8c46841b4d9176661156582b2548d244
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 31, 2015
- Expiry Date
- Jul 31, 2025
About this record
Access comprehensive regulatory information for Yingfang Rapid Test Reagent for Influenza A/B (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8c46841b4d9176661156582b2548d244 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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