Taiwan FDA registration 949198912635f1e2e8d94e958a6c10f1
“IF” Manual Polybrene Reagent
TW: “瑩芳” 凝聚胺聚合試劑
Taiwan·Risk Class 2·MD·Yingfang Co., Ltd. Taichung Factory·Registered Oct 20, 2014 – Oct 20, 2024ExpiredRegistration details
- Analysis ID
- 949198912635f1e2e8d94e958a6c10f1
- License Form
- Ministry of Health Medical Device Manufacturing No. 004712
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- The polyvalent cationic polymer in the agglutinous amine polymerization reagent was used to enhance the agglutination reaction between plasma antibodies and red blood cell antigens in a low-ion solution.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9300 Coomb automated test system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 20, 2014
- Expiry Date
- Oct 20, 2024
About this record
Access comprehensive regulatory information for “IF” Manual Polybrene Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 949198912635f1e2e8d94e958a6c10f1 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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