Dry Powder Inhaler - ANVISA Registration 80835239003

Access comprehensive regulatory information for Dry Powder Inhaler in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80835239003 and manufactured by PLASTIAPE S.P.A. ITALY. The registration is held by COSMED INDUSTRIA DE COSMETICOS E MEDICAMENTOS S.A. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including EMPHASYS IMPORTADORA EXPORTADORA E DISTRIBUIDORA LTDA, MANNKIND CORPORATION, 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.