Reinfusion Bag - ANVISA Registration 80588390003

Access comprehensive regulatory information for Reinfusion Bag in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80588390003 and manufactured by Puregraft LLC. The registration is held by ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including BIMINI HEALTH TECH, STRYKER MEDICAL, 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.