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SISTEMA DE CONFIRMACIÓN Y LOCALIZACIÓN DE LA PUNTA DE CATÉTERES CENTRALES INSERTADOS PERIFÉRICAMENTE, PARA MONITOREO CARDIACO - COFEPRIS Registration 1709E2024 SSA

Access comprehensive regulatory information for SISTEMA DE CONFIRMACIÓN Y LOCALIZACIÓN DE LA PUNTA DE CATÉTERES CENTRALES INSERTADOS PERIFÉRICAMENTE, PARA MONITOREO CARDIACO (SISTEMA DE CONFIRMACIÓN Y LOCALIZACIÓN DE LA PUNTA DE CATÉTERES CENTRALES INSERTADOS PERIFÉRICAMENTE, PARA MONITOREO CARDIACO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1709E2024 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on June 17, 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
1709E2024 SSA
SISTEMA DE CONFIRMACIÓN Y LOCALIZACIÓN DE LA PUNTA DE CATÉTERES CENTRALES INSERTADOS PERIFÉRICAMENTE, PARA MONITOREO CARDIACO
COFEPRIS Analysis ID: 1709E2024 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)
SHERLOCK 3CG+™
Trade Name (English)
SHERLOCK 3CG+™
Registration Information
Analysis ID
1709E2024 SSA
Registration Date
June 17, 2024
Manufacturer / Fabricante
Name (English)
BECTON DICKINSON DE MÉXICO, S.A. DE C.V.