PRESTIGE LPTM CERVICAL DISC - COFEPRIS Registration 1181C2019 SSA
Access comprehensive regulatory information for PRESTIGE LPTM CERVICAL DISC (PRESTIGE LPTM CERVICAL DISC) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1181C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on May 29, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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 DISCO CERVICAL PRESTIGE LPTM ESTÁ INDICADO PARA PACIENTES CON UN ESQUELETO MADURO PARA LA RECONSTRUCCIÓN DEL DISCO DESDE C3-C7 TRAS DISECTOMÍA A UN NIVEL O DOS NIVELES CONTIGUOS PARA RADICULOPATÍAS RESISTENTES AL TRATAMIENTO (DOLOR EN EL BRAZO Y/O DÉFI
THE PRESTIGE LPTM CERVICAL DISC IS INDICATED FOR PATIENTS WITH A MATURE SKELETON FOR DISC RECONSTRUCTION FROM C3-C7 AFTER DISCECTOMY AT ONE OR TWO CONTIGUOUS LEVELS FOR REFRACTORY RADICULOPATHIES (ARM PAIN AND/OR DEFICIENCY).