Intragastric Balloon - ANVISA Registration 10102180102

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 10102180102 and manufactured by SILIMED - INDÚSTRIA DE IMPLANTES LTDA. The registration is held by SILIMED - INDÚSTRIA DE IMPLANTES LTDA with validity until Nov 04, 2028.

This page provides complete technical specifications for this device, 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.