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SISTEMA DE DIATERMIA ELECTROQUIRÚRGICO DE USO GENERAL - COFEPRIS Registration 1270E2024 SSA

Access comprehensive regulatory information for SISTEMA DE DIATERMIA ELECTROQUIRÚRGICO DE USO GENERAL (SISTEMA DE DIATERMIA ELECTROQUIRÚRGICO DE USO GENERAL) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1270E2024 SSA and manufactured by EMERGO S. DE R.L. DE C.V.. The device was registered on May 03, 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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Clase II
1270E2024 SSA
SISTEMA DE DIATERMIA ELECTROQUIRÚRGICO DE USO GENERAL
COFEPRIS Analysis ID: 1270E2024 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)
CELLFX® SYSTEM.
Trade Name (English)
CELLFX® SYSTEM.
Registration Information
Analysis ID
1270E2024 SSA
Registration Date
May 03, 2024
Manufacturer / Fabricante
Name (English)
EMERGO S. DE R.L. DE C.V.