HYBRID WIRE - COFEPRIS Registration 886C2019 SSA
Access comprehensive regulatory information for HYBRID WIRE (HYBRID WIRE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 886C2019 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on April 30, 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.
DISPOSITIVO QUE SE UTILIZA PARA FACILITAR LA COLOCACIÓN DE CATÉTERES PARA USO DIAGNÓSTICO O TERAPÉUTICO EN EL ÁRBOL VASCULAR INTRACRANEAL
DEVICE USED TO FACILITATE PLACEMENT OF CATHETERS FOR DIAGNOSTIC OR THERAPEUTIC USE IN THE INTRACRANIAL VASCULAR TREE