VERSARIO® MULTIFOCAL 3F - COFEPRIS Registration 106C2019 SSA
Access comprehensive regulatory information for VERSARIO® MULTIFOCAL 3F (VERSARIO® MULTIFOCAL 3F) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 106C2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on January 29, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
ESTÁN INDICADAS PARA LA IMPLANTACIÓN PRIMARIA CON EL FIN DE CORREGIR PROBLEMAS DE VISIÓN COMO LA AFAQUIA TRAS LA EXTRACCIÓN DE UN CRISTALINO CATARATOSO EN PACIENTES ADULTOS, CON Y SIN PRESBICIA, QUE DESEAN UNA VISIÓN DE CERCA, INTERMEDIA Y DE LEJOS CON MA
THEY ARE INDICATED FOR PRIMARY IMPLANTATION IN ORDER TO CORRECT VISION PROBLEMS SUCH AS APHAKIA AFTER THE REMOVAL OF A CATARATE LENS IN ADULT PATIENTS, WITH AND WITHOUT PRESBYOPIA, WHO WANT NEAR, INTERMEDIATE AND DISTANCE VISION WITH MA.