Dry Powder Inhaler - ANVISA Registration 80978879001

Access comprehensive regulatory information for Dry Powder Inhaler in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80978879001 and manufactured by CIPLA LIMITED. The registration is held by CIPLA BRASIL IMPORTADORA E DISTRIBUIDORA DE MEDICAMENTOS LTDA 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, PLASTIAPE S.P.A. ITALY, 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.