Teryleaf Sendo Denture Adhesive (Non-Sterile) - Taiwan Registration fb0214eb03ad16cfae6e4e9dae42a9c2

Access comprehensive regulatory information for Teryleaf Sendo Denture Adhesive (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 fb0214eb03ad16cfae6e4e9dae42a9c2 and manufactured by NIPPON ZETTOC CO., LTD.. The authorized representative in Taiwan is CHUNG MEI BIOPHARMA 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.