Nephrostomy Set - ANVISA Registration 80160409041

Access comprehensive regulatory information for Nephrostomy Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80160409041 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 AMECO MEDICAL INDUSTRIES, COOK INCORPORATED, 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.