INFUSION DEVICE - ANVISA Registration 80312279031

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 80312279031 and manufactured by TELEFLEX MEDICAL EUROPE LIMITED. The registration is held by TELEFLEX MEDICAL 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 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.