BEXCKER AND DUET - COFEPRIS Registration 342C2019 SSA
Access comprehensive regulatory information for BEXCKER AND DUET (BEXCKER AND DUET) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 342C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on February 20, 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 DISPOSITIVO BECKER AND DUET ESTÁ INDICADO PARA EL DRENAJE Y MONITOREO DEL FLUJO DE LÍQUIDO CEFALORRAQUÍDEO (LCR) DESDE LOS VENTRÍCULOS LATERALES O EL ESPACIO SUBARACNOIDEO LUMBAR Y ES UTILIZADO EN PACIENTES SELECCIONADOS PARA: - REDUCIR LA PRESIÓN IN
THE BECKER AND DUET DEVICE IS INDICATED FOR DRAINAGE AND MONITORING OF CEREBROSPINAL FLUID (CSF) FLOW FROM THE LATERAL VENTRICLES OR LUMBAR SUBARACHNOID SPACE AND IS USED IN SELECTED PATIENTS TO: - REDUCE PRESSURE IN