Mexico COFEPRIS registration 1755C2019 SSA

ANAXTM 5.5 MIS SPINAL SYSTEM

EN: ANAXTM 5.5 MIS SPINAL SYSTEM
Mexico flagMexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·EMERGO S. DE R.L. DE C.V.·Registered August 27, 2019
Product Use / Uso del Producto
Spanish

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

English

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

Device classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
SISTEMA DE FIJACIÓN ESPINAL
Trade Name (English)
SPINAL FIXATION SYSTEM
Registration information
Analysis ID
1755C2019 SSA
Registration Date
August 27, 2019
Manufacturer / Fabricante
Name (English)
EMERGO S. DE R.L. DE C.V.
About this record

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.

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