"SEIKEN"QuickNavi-Norovirus 2 - Taiwan Registration 68175eb361b6b25704b8f779b15cf668

Access comprehensive regulatory information for "SEIKEN"QuickNavi-Norovirus 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68175eb361b6b25704b8f779b15cf668 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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.