Reinfusion Bag - ANVISA Registration 80005430376

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 80005430376 and manufactured by STRYKER MEDICAL. The registration is held by STRYKER DO BRASIL 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 Puregraft LLC, BIMINI HEALTH TECH, 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.