Taiwan FDA registration 1d654be94cafa8ee465b433133bf866b
"Yingfang" streptococcal latex detection reagent (unsterilized)
TW: "瑩芳"鏈球菌乳膠檢測試劑(未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Mar 23, 2011 – Mar 23, 2026ExpiredRegistration details
- Analysis ID
- 1d654be94cafa8ee465b433133bf866b
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Yingfang Co., Ltd. Taichung Factory
Product details
- Intended Use
- Classification and grading management method of medical equipment: Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 23, 2011
- Expiry Date
- Mar 23, 2026
About this record
Access comprehensive regulatory information for "Yingfang" streptococcal latex detection 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 1d654be94cafa8ee465b433133bf866b and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is Yingfang Co., Ltd. Taichung Factory.
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