SPACER - ANVISA Registration 81230160003

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81230160003 and manufactured by VISIOMED TECHNOLOGY CO., LTD.. The registration is held by VISIOMED DO BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA - ME 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 PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA, HUIZHOU KAIYI TECHNOLOGY CO.,LTD, 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.