SISTEMA DE CONFIRMACIÓN Y LOCALIZACIÓN DE LA PUNTA DE CATÉTERES CENTRALES INSERTADOS PERIFÉRICAMENTE, PARA MONITOREO CARDIACO
Mexico·Clase II·I. Equipo Médico·BECTON DICKINSON DE
MÉXICO, S.A. DE C.V.·Registered June 17, 2024- 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+™
- Analysis ID
- 1709E2024 SSA
- Registration Date
- June 17, 2024
- Name (Spanish)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
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.