Taiwan FDA registration 36c7dfb3833d2a9bae4b8d32a8e7f1f5
“IF” Antibody Screening Cell
TW: “瑩芳”抗體篩檢細胞組
Taiwan·Risk Class 2·MD·Yingfang Co., Ltd. Taichung Factory·Registered Jul 29, 2015 – Jul 29, 2025ExpiredRegistration details
- Analysis ID
- 36c7dfb3833d2a9bae4b8d32a8e7f1f5
- License Form
- Ministry of Health Medical Device Manufacturing No. 004947
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- This product is used to screen for red blood cell antibodies in plasma (clear) samples.
- 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
- Jul 29, 2015
- Expiry Date
- Jul 29, 2025
About this record
Access comprehensive regulatory information for “IF” Antibody Screening Cell in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36c7dfb3833d2a9bae4b8d32a8e7f1f5 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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