Intragastric Balloon - ANVISA Registration 80991380012

Access comprehensive regulatory information for Intragastric Balloon in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80991380012 and manufactured by HELIOSCOPIE S. A.. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO LTDA with validity until Aug 13, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDICONE PROJETOS E SOLUÇÕES PARA A INDÚSTRIA E A SAÚDE LTDA, APOLLO ENDOSURGERY, INC, 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.