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. 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.