VAGINAL PH SELF-TEST - ANVISA Registration 80113770052

Access comprehensive regulatory information for VAGINAL PH SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80113770052 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including CHEMBIO DIAGNOSTICS BRAZIL LTDA., and 1 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.