Headlight - ANVISA Registration 80073250043

Access comprehensive regulatory information for Headlight in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80073250043 and manufactured by QED INC.. The registration is held by M Z PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including QED INC., ZUMAX MEDICAL CO, LTD., 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.