FERTILITY SELF-TEST INSTRUMENT - ANVISA Registration 82195300004

Access comprehensive regulatory information for FERTILITY SELF-TEST INSTRUMENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82195300004 and manufactured by SEJOY BIOMEDICAL CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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.