EXCELSIOR. - COFEPRIS Registration 1316C2019 SSA
Access comprehensive regulatory information for EXCELSIOR. (EXCELSIOR.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1316C2019 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on July 16, 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.
EL MICROCATÉTER EXCELSIOR DE STRYKER NEUROVASCULAR ESTÁ INDICADO PARA FACILITAR LA INTRODUCCIÓN DE AGENTES DE DIAGNOSTICO (COMO MEDIOS DE CONTRASTE) Y AGENTES TERAPÉUTICOS (COMO ESPIRALES DE OCLUSIÓN) EN LA VASCULATURA PERIFÉRICA, CORONARIA Y DEL SISTEMA
THE STRYKER NEUROVASCULAR EXCELSIOR MICROCATHETER IS INDICATED TO FACILITATE THE INTRODUCTION OF DIAGNOSTIC AGENTS (SUCH AS CONTRAST MEDIA) AND THERAPEUTIC AGENTS (SUCH AS OCCLUSION COILS) INTO THE PERIPHERAL, CORONARY AND SYSTEM VASCULATURE.