Mexico COFEPRIS registration 1181C2019 SSA

PRESTIGE LPTM CERVICAL DISC

EN: PRESTIGE LPTM CERVICAL DISC
Mexico flagMexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·MEDTRONIC, S. DE R.L. DE C.V.·Registered May 29, 2019
Product Use / Uso del Producto
Spanish

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

English

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).

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 DISCOS CERVICALES
Trade Name (English)
CERVICAL DISC SYSTEM
Registration information
Analysis ID
1181C2019 SSA
Registration Date
May 29, 2019
Manufacturer / Fabricante
Name (English)
MEDTRONIC, S. DE R.L. DE C.V.
About this record

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.

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