"Artron" Helicobacter pylori (HP) Antigen Rapid Test (Non-Sterile) - Taiwan Registration 410c4c23ed7ecf141b59fd420e3cc4c5

Access comprehensive regulatory information for "Artron" Helicobacter pylori (HP) Antigen Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 410c4c23ed7ecf141b59fd420e3cc4c5 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY 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.