“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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Device Details
Registration Details
d0888df264f3f0fc4edac94c920f90a2
Ministry of Health Medical Device Manufacturing No. 004728
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

