Devices for Female Contraception - ANVISA Registration 10208250050

Access comprehensive regulatory information for Devices for Female Contraception in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10208250050 and manufactured by KESSEL MEDINTIM GMBH. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA with validity until Mar 28, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 companies making the same product including SEMINA INDÚSTRIA E COMÉRCIO LTDA, SMB CORPORATION OF INDIA, 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.