Resin Polymerization Device - ANVISA Registration 80117581102

Access comprehensive regulatory information for Resin Polymerization Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80117581102 and manufactured by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including IVOCLAR VIVADENT AG, SDI LIMITED, 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.