FARGO - COFEPRIS Registration 1084C2019 SSA
Access comprehensive regulatory information for FARGO (FARGO) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1084C2019 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on May 21, 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.
LOS CATÉTERES GUÍA ESTÁN IDEADOS PARA FACILITAR LA COLOCACIÓN DE LOS MICROCATÉTERES PARA USO TERAPÉUTICO Y DIAGNÓSTICO EN INTERVENCIONES NEUROLÓGICAS.
GUIDE CATHETERS ARE DESIGNED TO FACILITATE THE PLACEMENT OF MICROCATHETERS FOR THERAPEUTIC AND DIAGNOSTIC USE IN NEUROLOGICAL INTERVENTIONS.