Dry Powder Inhaler - ANVISA Registration 81244549003

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 81244549003 and manufactured by MANNKIND CORPORATION. The registration is held by BIOMM SA 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.