GLÚCOMETRO - COFEPRIS Registration 0319E2024 SSA
Access comprehensive regulatory information for GLÚCOMETRO (GLÚCOMETRO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0319E2024 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on January 30, 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 I
0319E2024 SSA
GLÚCOMETRO
COFEPRIS Analysis ID: 0319E2024 SSA
Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
I-SENS, SISTEMA DE
MONITOREO DE GLUCOSA
EN SANGRE
Trade Name (English)
I-SENS, SISTEMA DE
MONITOREO DE GLUCOSA
EN SANGRE
Registration Information
Analysis ID
0319E2024 SSA
Registration Date
January 30, 2024
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.Name (English)
AXMILAB, S.A. DE C.V.