VIBEX XTRA. - COFEPRIS Registration 184C2018 SSA
Access comprehensive regulatory information for VIBEX XTRA. (VIBEX XTRA.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 184C2018 SSA and manufactured by ARFAMEX, S.A. DE C.V.. The device was registered on January 15, 2018.
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.
PARA EL ENDURECIMIENTO CORNEAL, DESPUÉS DE REMOVER EL EPITELIO O SOBRE LA BASE DE ESTROMA. EXCLUSIVAMENTE PARA USO OFTÁLMICO, NO INYECTAR.
FOR CORNEAL HARDENING, AFTER REMOVING THE EPITHELIUM OR ON THE STROMAL BASIS. FOR OPHTHALMIC USE ONLY, DO NOT INJECT.