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ELECTRODOS DE DESFIBRILADOR - COFEPRIS Registration 0607E2024 SSA

Access comprehensive regulatory information for ELECTRODOS DE DESFIBRILADOR (ELECTRODOS DE DESFIBRILADOR) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0607E2024 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on March 01, 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
0607E2024 SSA
ELECTRODOS DE DESFIBRILADOR
COFEPRIS Analysis ID: 0607E2024 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)
VERMED HEARTSYNC
Trade Name (English)
VERMED HEARTSYNC
Registration Information
Analysis ID
0607E2024 SSA
Registration Date
March 01, 2024
Manufacturer / Fabricante
Name (English)
MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.