INFUSION DEVICE - ANVISA Registration 80808489033

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 80808489033 and manufactured by ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD.. The registration is held by BECARE COMÉRCIO DE PRODUTOS MÉDICO HOSPITALARES LTDA EPP 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 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.