BAUSCH + LOMB® BIOTRUE ONEDAY (NESOFILCON A) PARA PRESBICIA - COFEPRIS Registration 1288C2018 SSA
Access comprehensive regulatory information for BAUSCH + LOMB® BIOTRUE ONEDAY (NESOFILCON A) PARA PRESBICIA (BAUSCH + LOMB® BIOTRUE ONEDAY (NESOFILCON A) FOR PRESBYOPIA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1288C2018 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 (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.
EL LENTE DE CONTACTO HIDROFÍLICO BAUSCH + LOMB® BIOTRUE ONEDAY (NESOFILCON A) PARA PRESBICIA, ESTÁ INDICADO PARA USO DIARIO PARA LA CORRECCIÓN DE LA AMETROPÍA REFRACTIVA (MIOPÍA, HIPERMETROPÍA Y ASTIGMATISMO) EN PERSONAS AFÁQUICAS Y/O NO AFÁQUICAS SIN ENF
THE BAUSCH + LOMB® BIOTRUE ONEDAY HYDROPHILIC CONTACT LENS (NESOFILCON A) FOR PRESBYOPIA, IS INDICATED FOR DAILY USE FOR THE CORRECTION OF REFRACTIVE AMETROPIA (MYOPIA, HYPEROPIA AND ASTIGMATISM) IN APHAKIC AND / OR NON-APHAKIC PEOPLE WITHOUT ENF.