FLOWGATE2™ - COFEPRIS Registration 1985C2018 SSA
Access comprehensive regulatory information for FLOWGATE2™ (FLOWGATE2™) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1985C2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on August 10, 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.
LOS CATÉTERES GUÍA CON BALÓN FLOWGATE2™ ESTÁN INDICADOS PARA FACILITAR LA INTRODUCCIÓN Y GUÍA DE UN CATÉTER INTRAVASCULAR EN UN VASO SANGUÍNEO SELECCIONADO DE LOS SISTEMAS PERIFÉRICO Y NEUROVASCULAR. EL BALÓN PROPORCIONA UNA OCLUSIÓN VASCULAR TEMPORAL DUR
FLOWGATE2™ BALLOON GUIDE CATHETERS ARE INDICATED TO FACILITATE THE INTRODUCTION AND GUIDANCE OF AN INTRAVASCULAR CATHETER INTO A SELECTED BLOOD VESSEL OF THE PERIPHERAL AND NEUROVASCULAR SYSTEMS. THE BALLOON PROVIDES A DUR TEMPORARY VASCULAR OCCLUSION