Dry Powder Inhaler - ANVISA Registration 81352749001

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 81352749001 and manufactured by EMPHASYS IMPORTADORA EXPORTADORA E DISTRIBUIDORA LTDA. The registration is held by EUROFARMA LABORATÓRIOS S.A with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 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.