Cold Light Source - ANVISA Registration 80082919062

Access comprehensive regulatory information for Cold Light Source in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80082919062 and manufactured by MDKMED MEDICAL TECHNOLOGY CO., LTD.. The registration is held by CIENLABOR INDUSTRIA E COMERCIO 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 RICHARD WOLF GMBH, INNOVA TECHNIK IMPORTAÇÃO E EXPORTAÇÃO LTDA, 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.