Infusion/injection devices - ANVISA Registration 80520099027

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 80520099027 and manufactured by LMG LASERS - COMERCIO, IMPORTACAO E EXPORTACAO LTDA. The registration is held by LMG LASERS - COMERCIO, IMPORTACAO E EXPORTACAO 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 AEROPHARM GMBH, 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.