HEALON DUET PRO - COFEPRIS Registration 1865C2019 SSA
Access comprehensive regulatory information for HEALON DUET PRO (HEALON DUET PRO) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1865C2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on September 13, 2019.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
ESTÁ DISEÑADO PARA PROPORCIONAR DOS PRODUCTOS VISCOELÁSTICOS CON CARACTERÍSTICAS FISIOQUÍMICAS DIFERENTES QUE PUEDEN UTILIZARSE COMBINADOS PARA REALIZAR TAREAS ESPECÍFICAS DURANTE LA INTERVENCIÓN QUIRÚRGICA DE CATARATAS. PARA CIRUGÍA OCULAR. EN PROCEDIMIE
IT IS DESIGNED TO PROVIDE TWO VISCOELASTIC PRODUCTS WITH DIFFERENT PHYSIOCHEMICAL CHARACTERISTICS THAT CAN BE USED IN COMBINATION TO PERFORM SPECIFIC TASKS DURING CATARACT SURGERY. FOR EYE SURGERY. IN PROCEDURE