Mexico COFEPRIS registration 2072E2019 SSA

MAGNETOM ALTEA

EN: ALTEA MAGNET

Mexico·Clase II·I. MEDICAL EQUIPMENT·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered November 01, 2019

Product Use / Uso del Producto

Spanish

PAA USO DE DIAGNOSTICO POR RESONANCIA MAGNETICA

English

PAA USE OF MAGNETIC RESONANCE DIAGNOSTICS

Device classification

Risk Class / Clase de Riesgo: Clase II
Product Type (Spanish): I. EQUIPO MÉDICO
Product Type (English): I. MEDICAL EQUIPMENT
Trade Name (Spanish): SITEMA DE IMAGENOLOGIA POR RESONANCIA MAGNETICA
Trade Name (English): MAGNETIC RESONANCE IMAGING SYSTEM

Registration information

Analysis ID: 2072E2019 SSA
Registration Date: November 01, 2019

Manufacturer / Fabricante

Name (Spanish): SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
Name (English): SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR

About this record

Access comprehensive regulatory information for MAGNETOM ALTEA (ALTEA MAGNET) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2072E2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on November 01, 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.

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