ARTELAC® COMPLETE MDO®. - COFEPRIS Registration 1043C2019 SSA
Access comprehensive regulatory information for ARTELAC® COMPLETE MDO®. (ARTELAC® COMPLETE MDO®.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1043C2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on May 16, 2019.
This page provides complete registration details including product type (VI. HYGIENIC PRODUCTS), 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.
ARTELAC® COMPLETE MDO® ES UN LUBRICANTE OCULAR QUE CONTRIBUYE AL MANTENIMIENTO DE LAS TRES CAPAS DE LA PELÍCULA LAGRIMAL (LIPÍDICA, ACUOSA Y MUCÍNICA) PARA MEJORAR LA HUMECTACIÓN DE LA SUPERFICIE OCULAR CUANDO HAY SENSACIÓN DE OJO SECO.
ARTELAC® COMPLETE MDO® IS AN EYE LUBRICANT THAT CONTRIBUTES TO THE MAINTENANCE OF THE THREE LAYERS OF THE TEAR FILM (LIPID, AQUEOUS AND MUCINIC) TO IMPROVE THE MOISTURIZATION OF THE OCULAR SURFACE WHEN THERE IS A DRY EYE SENSATION.