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“IF” Antibody Screening Cell - Taiwan Registration 36c7dfb3833d2a9bae4b8d32a8e7f1f5

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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36c7dfb3833d2a9bae4b8d32a8e7f1f5
Registration Details
Taiwan FDA Registration: 36c7dfb3833d2a9bae4b8d32a8e7f1f5
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Device Details

“IF” Antibody Screening Cell
TW: “瑩芳”抗體篩檢細胞組
Risk Class 2
MD

Registration Details

36c7dfb3833d2a9bae4b8d32a8e7f1f5

Ministry of Health Medical Device Manufacturing No. 004947

Company Information

Taiwan, Province of China

Product Details

This product is used to screen for red blood cell antibodies in plasma (clear) samples.

B Hematology and pathology devices

B9300 Coomb automated test system

Produced in Taiwan, China

Dates and Status

Jul 29, 2015

Jul 29, 2025