BAUSCH + LOMB(R) BIOTURE ONEDAY (NESOFILCON A) - COFEPRIS Registration 275C2018 SSA
Access comprehensive regulatory information for BAUSCH + LOMB(R) BIOTURE ONEDAY (NESOFILCON A) (BAUSCH + LOMB(R) BIOTURE ONEDAY (NESOFILCON A)) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 275C2018 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on January 29, 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.
INDICADO PARA USO DIARIO PARA LA CORRECCIÓN DE AMETROPÍAS DE REFACCIÓN (MIOPÍA, HIPERMETROPIA Y ASTIGMATISMO) EN PERSONAS AFÁQUICAS Y/O NO AFÁQUICAS SIN ENFERMEDAD EN LOS OJOS, MOSTRANDO ASTIGMATISMO DE 2.00 DIOPTRÍAS O MENOS, QUE NO INTERFIERA CON LA AGU
INDICATED FOR DAILY USE FOR THE CORRECTION OF SPARE AMETROPIA (MYOPIA, HYPEROPIA AND ASTIGMATISM) IN APHAKIC AND / OR NON-APHAKIC PEOPLE WITHOUT EYE DISEASE, SHOWING ASTIGMATISM OF 2.00 DIOPTERS OR LESS, WHICH DOES NOT INTERFERE WITH WATER