Filtration Line - ANVISA Registration 81971219001

Access comprehensive regulatory information for Filtration Line in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81971219001 and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD. The registration is held by JM VELLAME COMERCIO, REPRESENTACAO, LOCACAO E MANUTENCAO DE EQUIPAMENTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including GAMBRO DASCO S.P.A, and 1 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.