Kit for Infusion Pump - ANVISA Registration 80804050198

Access comprehensive regulatory information for Kit for Infusion Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80804050198 and manufactured by Bemis Manufacturing Company. The registration is held by Smith & Nephew Comércio de Produtos Médicos 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 SHANDONG ANDE HEALTHCARE APPARATUS CO., LTD., SHENZHEN MAIWEI BIOTECH CO., LTD., 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.