Yingfang Rapid Test Reagent for Influenza A/B (Unsterilized) - Taiwan Registration 8c46841b4d9176661156582b2548d244
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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Device Details
Product Details
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.
C Immunology and microbiology
C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
Domestic
Dates and Status
Jul 31, 2015
Jul 31, 2025