URINARY STENT - ANVISA Registration 80160409040

Access comprehensive regulatory information for URINARY STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80160409040 and manufactured by HUNAN REBORN MEDICAL SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD. The registration is held by ASHER-SILB MEDICAL DO 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 BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, BOSTON SCIENTIFIC CORPORATION, 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.