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“IF” RPR (RPR Antigen) Test for Syphilis - Taiwan Registration d0888df264f3f0fc4edac94c920f90a2

Access comprehensive regulatory information for “IF” RPR (RPR Antigen) Test for Syphilis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d0888df264f3f0fc4edac94c920f90a2 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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d0888df264f3f0fc4edac94c920f90a2
Registration Details
Taiwan FDA Registration: d0888df264f3f0fc4edac94c920f90a2
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Device Details

“IF” RPR (RPR Antigen) Test for Syphilis
TW: “瑩芳” 梅毒檢測試劑組
Risk Class 2
MD

Registration Details

d0888df264f3f0fc4edac94c920f90a2

Ministry of Health Medical Device Manufacturing No. 004728

Company Information

Taiwan, Province of China

Product Details

Detection of nonspecific treponemal antibodies in serum or plasma.

C Immunology and microbiology devices

C3820 Treponemal pallidum non-treponemal reagent

Produced in Taiwan, China

Dates and Status

Nov 10, 2014

Nov 10, 2024