Extractor - ANVISA Registration 80320689018

Access comprehensive regulatory information for Extractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80320689018 and manufactured by JIANGSU RIPE MEDICAL INSTRUMENTS TECHNOLOGY CO. LTD.. The registration is held by DANIALEX TEC - MATERIAL MEDICO HOSPITALAR LTDA ME 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.