Blood Filter/Arterial Filter - ANVISA Registration 80788629001

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 80788629001 and manufactured by DONGGUAN KEWEI MEDICAL INSTRUMENT CO. LTD.. The registration is held by NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MEDTRONIC, INC., CARDIO MEDICAL INDUSTRIAL LTDA, 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.