Adhesion/Silanization Agent - ANVISA Registration 80284930232

Access comprehensive regulatory information for Adhesion/Silanization Agent in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80284930232 and manufactured by 3M ESPE AG. The registration is held by 3M DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 4 related devices, regulatory compliance details, 5 companies making the same product including DENTSPLY IND.COM. LTDA, SHOFU INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.