VACUUM WOUND THERAPY SYSTEM - ANVISA Registration 10306849022

Access comprehensive regulatory information for VACUUM WOUND THERAPY SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10306849022 and manufactured by GENADYNE BIOTECHNOLOGIES INC.. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO 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 KCI USA, INC., SMITH & NEPHEW MEDICAL 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.