Semen/Sperm Analysis - ANVISA Registration 81189660108

Access comprehensive regulatory information for Semen/Sperm Analysis in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81189660108 and manufactured by ACMEX BIO-TECHNOLOGY (CHONGQING) CO., LTD.. The registration is held by SÓLIDA HOSPITALAR - DISTRIBUIDORA DE MATERIAL HOSPITALAR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.