"Yingfang" Helicobacter pylori rapid test reagent (unsterilized) - Taiwan Registration ca0d1c07fec57522de7ff83c2aaa8bdf
Access comprehensive regulatory information for "Yingfang" Helicobacter pylori rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca0d1c07fec57522de7ff83c2aaa8bdf 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.
Device Details
Product Details
Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
C Immunology and microbiology
C.0003 ่บๆๆกฟ่ๅฑฌ่กๆธ ่ฉฆๅ
Domestic
Dates and Status
Jul 15, 2011
Jul 15, 2026

