STELLARIS ELITE™ - COFEPRIS Registration 1287E2018 SSA
Access comprehensive regulatory information for STELLARIS ELITE™ (STELLARIS ELITE™) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1287E2018 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on June 01, 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.
INDICADO PARA LA EMULSIFICACIÓN Y EXTRACCIÓN DE CATARATAS Y PARA VITRECTOMÍAS EN INTERVENCIONES QUIRÚRGICAS DE LOS SEGMENTOS ANTERIOR Y POSTERIOR. EL SISTEMA ESTÁ DISEÑADO PARA UTILIZARSE EN INTERVENCIONES TANTO DEL SEGMENTO ANTERIOR COMO DEL SEGMENTO POS
INDICATED FOR THE EMULSIFICATION AND EXTRACTION OF CATARACTS AND FOR VITRECTOMIES IN SURGICAL INTERVENTIONS OF THE ANTERIOR AND POSTERIOR SEGMENTS. THE SYSTEM IS DESIGNED FOR USE IN BOTH ANTERIOR AND POS SEGMENT INTERVENTIONS.