MAGNETOM LUMINA
Mexico·Clase II·I. MEDICAL EQUIPMENT·SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.·Registered September 03, 2019EL SISTEMA MAGNETOM LUMINA ESTÁ INDICADO PARA SU USO COMO DISPOSITIVO DE DIAGNÓSTICO POR RESONANCIA MAGNÉTICA (DDRM). PRODUCE IMÁGENES DE CORTES TRANSVERSALES, SAGITALES, CORONALES Y OBLICUOS, E IMÁGENES ESPECTROSCÓPICAS O ESPECTROS, Y MUESTRA LA ESTRUCTU
THE MAGNETOM LUMINA SYSTEM IS INDICATED FOR USE AS A MAGNETIC RESONANCE DIAGNOSTIC (DDRM) DEVICE. PRODUCES CROSS-SECTION, SAGITTAL, CORONAL AND OBLIQUE IMAGES, AND SPECTROSCOPIC IMAGES OR SPECTRA, AND DISPLAYS THE STRUCTURE
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- SISTEMA DE IMAGENOLOGÍA POR RESONANCIA MAGNÉTICA
- Trade Name (English)
- MAGNETIC RESONANCE IMAGING SYSTEM
- Analysis ID
- 1806E2019 SSA
- Registration Date
- September 03, 2019
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
Access comprehensive regulatory information for MAGNETOM LUMINA (MAGNETOM LUMINA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1806E2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on September 03, 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.