COPERNIC - COFEPRIS Registration 1814C2018 SSA
Access comprehensive regulatory information for COPERNIC (COPERNICUS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1814C2018 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on July 26, 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.
DISPOSITIVO INDICADO PARA SU USO EN EL SISTEMA NEUROVASCULAR Y PERIFÉRICO, A FIN DE DETENER O CONTROLAR EL FLUJO SANGUÍNEO, PARA TRATAR VASOESPASMOS Y PARA LA EMBOLIZACIÓN DE ANEURISMAS ASISTIDA CON BALÓN.
A DEVICE INDICATED FOR USE IN THE NEUROVASCULAR AND PERIPHERAL SYSTEM, TO STOP OR CONTROL BLOOD FLOW, TO TREAT VASOSPASMS, AND FOR BALLOON-ASSISTED EMBOLIZATION OF ANEURYSMS.