ECLIPSE - COFEPRIS Registration 1811C2018 SSA
Access comprehensive regulatory information for ECLIPSE (ECLIPSE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1811C2018 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 USO EN EL SISTEMA NEUROVASCULAR Y PERIFÉRICO, A FIN DE DETERNER O CONTROLAR TEMPORALMENTE EL FLUJO SANGUÍNEO, PARA TRATAV VASOESPASMOS Y PARA LA EMBOLIZACIÓN DE ANEURISMAS ASISTIDA POR BALÓN.
DEVICE INDICATED FOR USE IN THE NEUROVASCULAR AND PERIPHERAL SYSTEM, IN ORDER TO TEMPORARILY STOP OR CONTROL BLOOD FLOW, FOR VASOSPASMS AND FOR BALLOON-ASSISTED EMBOLIZATION OF ANEURYSMS.