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EQUIPO DE DIAGNÓSTICO POR ULTRASONIDO - COFEPRIS Registration 1157E2024 SSA

Access comprehensive regulatory information for EQUIPO DE DIAGNÓSTICO POR ULTRASONIDO (EQUIPO DE DIAGNÓSTICO POR ULTRASONIDO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1157E2024 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on April 22, 2024.

This page provides complete registration details including product type (I. Equipo Médico), 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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COFEPRIS Official Data
Clase II
1157E2024 SSA
EQUIPO DE DIAGNÓSTICO POR ULTRASONIDO
COFEPRIS Analysis ID: 1157E2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
SISTEMA DE ULTRASONIDO DE DIAGNÓSTICO (ACUSON P500)
Trade Name (English)
SISTEMA DE ULTRASONIDO DE DIAGNÓSTICO (ACUSON P500)
Registration Information
Analysis ID
1157E2024 SSA
Registration Date
April 22, 2024
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.