Infusion/injection devices - ANVISA Registration 80708690001

Access comprehensive regulatory information for Infusion/injection devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80708690001 and manufactured by AEROPHARM GMBH. The registration is held by SANDOZ DO BRASIL INDÚSTRIA FARMACÊUTICA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including LMG LASERS - COMERCIO, IMPORTACAO E EXPORTACAO LTDA, WUXI NEST BIOTECHNOLOGY CO., LTD., and 2 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.