Extractor - ANVISA Registration 80312270019

Access comprehensive regulatory information for Extractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80312270019 and manufactured by TELEFLEX MEDICAL INC. 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 RUSSER BRASIL LTDA, KARL STORZ SE & CO. KG, 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.