SISTEMA ESA BAUSCH + LOMB - COFEPRIS Registration 2110E2018 SSA
Access comprehensive regulatory information for SISTEMA ESA BAUSCH + LOMB (ESA BAUSCH + LOMB SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2110E2018 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on August 29, 2018.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
EL SISTEMA ESA BAUSCH + LOMB ES UN INSTRUMENTO QUIRÚRGICO MANUAL DESTINADO A SER UTILIZADO COMO TROCAR/CÁNULA PARA ESTABLECER UN CONDUCTO DE ENTRADA PARA EL PASO DE INSTRUMENTOS OFTÁLMICOS/ACCESORIOS UTILIZADOS PARA REALIZAR PROCEDIMIENTOS QUIRÚRGICOS OFT
THE ESA BAUSCH + LOMB SYSTEM IS A HANDHELD SURGICAL INSTRUMENT INTENDED TO BE USED AS A TROCAR/CANNULA TO ESTABLISH AN INLET DUCT FOR THE PASSAGE OF OPHTHALMIC INSTRUMENTS/ACCESSORIES USED TO PERFORM OFT SURGICAL PROCEDURES