Headlight - ANVISA Registration 10392999018

Access comprehensive regulatory information for Headlight in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10392999018 and manufactured by MK PRODUTOS PARA SAUDE LTDA. The registration is held by MK PRODUTOS PARA SAUDE 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.