INFUSION DEVICE - ANVISA Registration 81414021691

Access comprehensive regulatory information for INFUSION DEVICE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81414021691 and manufactured by ROCHE DIAGNOSTICS - GMBH. The registration is held by ROCHE DIABETES CARE BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SMITHS MEDICAL ASD, INC. (MINNEAPOLIS), UNOMEDICAL A/S, 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.