Blood Filter/Arterial Filter - ANVISA Registration 10349009045

Access comprehensive regulatory information for Blood Filter/Arterial Filter in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10349009045 and manufactured by MEDTRONIC, INC.. The registration is held by AUTO SUTURE DO BRASIL LTDA. 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 CARDIO MEDICAL INDUSTRIAL LTDA, FRESENIUS KABI AG, 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.