Assisted reproduction laser system - ANVISA Registration 83085839001

Access comprehensive regulatory information for Assisted reproduction laser system in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 83085839001 and manufactured by VITROLIFE GMBH. The registration is held by VITROLIFE BRASIL COMERCIO DE EQUIPAMENTOS LABORATORIAIS LTDA 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 VITROLIFE GMBH, 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.