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ANALIZADOR CLÍNICO POR MEDICION DIRECTA POR ELECTRODO SELECTIVO DE IONES NA+, K+, CL- Y LI+ - COFEPRIS Registration 0348E2022 SSA

Access comprehensive regulatory information for ANALIZADOR CLÍNICO POR MEDICION DIRECTA POR ELECTRODO SELECTIVO DE IONES NA+, K+, CL- Y LI+ (ANALIZADOR CLÍNICO POR MEDICION DIRECTA POR ELECTRODO SELECTIVO DE IONES NA+, K+, CL- Y LI+) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0348E2022 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on May 04, 2022.

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 I
0348E2022 SSA
ANALIZADOR CLÍNICO POR MEDICION DIRECTA POR ELECTRODO SELECTIVO DE IONES NA+, K+, CL- Y LI+
COFEPRIS Analysis ID: 0348E2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
PROLYTE®
Trade Name (English)
PROLYTE®
Registration Information
Analysis ID
0348E2022 SSA
Registration Date
May 04, 2022
Manufacturer / Fabricante
Name (Spanish)
DICIPA, S.A. DE C.V.
Name (English)
DICIPA, S.A. DE C.V.