ANAXTM 5.5 MIS SPINAL SYSTEM - COFEPRIS Registration 1755C2019 SSA
Access comprehensive regulatory information for ANAXTM 5.5 MIS SPINAL SYSTEM (ANAXTM 5.5 MIS SPINAL SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1755C2019 SSA and manufactured by EMERGO S. DE R.L. DE C.V.. The device was registered on August 27, 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 SISTEMA ESPINAL ANAX™ 5.5 MIS UN SISTEMA DE FIJACIÓN PEDICULAR POSTERIOR, PRETENDE PROVEER DE INMOVILIZACIÓN Y ESTABILIZACIÓN DE LOS SEGMENTOS ESPINALES EN COMPLEMENTO EN PACIENTES ESQUELÉTICAMENTE MADUROS COMO UN ADJUNTO PARA LA FUSIÓN POR HUESO AUTÓG
THE ANAX SPINAL™ SYSTEM 5.5 MIS A POSTERIOR PEDICLE FIXATION SYSTEM, AIMS TO PROVIDE IMMOBILIZATION AND STABILIZATION OF SPINAL SEGMENTS IN COMPLEMENT IN SKELETALLY MATURE PATIENTS AS AN ADJUNCT FOR FUSION BY AUTOLOGOUS BONE