INSTRUMENTAL PARA EL SISTEMA ARTIC-L™ 3D TI SPINAL SYSTEM - COFEPRIS Registration 607E2019 SSA
Access comprehensive regulatory information for INSTRUMENTAL PARA EL SISTEMA ARTIC-L™ 3D TI SPINAL SYSTEM (INSTRUMENTATION FOR THE ARTIC-L™ 3D TI SPINAL SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 607E2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on March 26, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 INSTRUMENTAL PARA EL SISTEMA ARTIC-L™ 3D TI SPINAL SYSTEM, ES INSTRUMENTAL GENERAL INDICADO PARA USARSE CON EL SISTEMA ESPINAL ARTIC-L™ 3D TI CON TECNOLOGÍA TIONIC™ EL CUAL ESTÁ DISEÑADO PARA SU USO COMO DISPOSITIVO DE FUSIÓN DE CUERPO INTERVERTEBRAL.
THE INSTRUMENTATION FOR THE ARTIC-L™ 3D TI SPINAL SYSTEM, IS GENERAL INSTRUMENTATION INDICATED FOR USE WITH THE ARTIC-L™ 3D TI SPINAL SYSTEM WITH TIONIC™ TECHNOLOGY WHICH IS DESIGNED FOR USE AS AN INTERVERTEBRAL BODY FUSION DEVICE.