Connectors - ANVISA Registration 80160719002

Access comprehensive regulatory information for Connectors in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80160719002 and manufactured by TIANCK MEDICAL CO., LTD. The registration is held by PMF CARDIOLIFE IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BMR MEDICAL S.A., SHANGHAI HEALTH MEDICAL 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.