Probes - ANVISA Registration 80199330009

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80199330009 and manufactured by R-VENT MEDIKAL URETIM A.S. The registration is held by DELF DISTRIBUIDORA DE MEDICAMENTOS 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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.