“Friadent” ANKYLOS Balance Abutment System - Taiwan Registration d9c295bc7b5e03a4263d64896ec9238a

Access comprehensive regulatory information for “Friadent” ANKYLOS Balance Abutment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d9c295bc7b5e03a4263d64896ec9238a and manufactured by DENTSPLY IMPLANTS MANUFACTURING GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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.