Taiwan FDA registration d0888df264f3f0fc4edac94c920f90a2
“IF” RPR (RPR Antigen) Test for Syphilis
TW: “瑩芳” 梅毒檢測試劑組
Taiwan·Risk Class 2·MD·Yingfang Co., Ltd. Taichung Factory·Registered Nov 10, 2014 – Nov 10, 2024ExpiredRegistration details
- Analysis ID
- d0888df264f3f0fc4edac94c920f90a2
- License Form
- Ministry of Health Medical Device Manufacturing No. 004728
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Detection of nonspecific treponemal antibodies in serum or plasma.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3820 Treponemal pallidum non-treponemal reagent
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 10, 2014
- Expiry Date
- Nov 10, 2024
About this record
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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices