MEDTRONIC RESERVORIOS 2 - COFEPRIS Registration 380C2019 SSA
Access comprehensive regulatory information for MEDTRONIC RESERVORIOS 2 (MEDTRONIC RESERVOIRS 2) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 380C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on February 27, 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 RESERVORIOS VENTRICULARES ESTÁN INDICADOS PARA PROPORCIONAR ACCESO PERCUTÁNEO AL LÍQUIDO CEFALORRAQUÍDEO (LCR) VENTRICULAR A TRAVÉS DE UN RESERVORIO DE ELASTÓMERO DE SILICONA CONECTADO A UN CATÉTER VENTRICULAR. LOS RESERVORIOS VENTRICULARES DE LÍQUID
VENTRICULAR RESERVOIRS ARE INDICATED TO PROVIDE PERCUTANEOUS ACCESS TO VENTRICULAR CEREBROSPINAL FLUID (CSF) THROUGH A SILICONE ELASTOMER RESERVOIR CONNECTED TO A VENTRICULAR CATHETER. LIQUID VENTRICULAR RESERVOIRS