Mexico COFEPRIS registration 1169E2024 SSA

DISPOSITIVO DE MONITOREO DE GLUCOSA EN SANGRE.

EN: DISPOSITIVO DE MONITOREO DE GLUCOSA EN SANGRE.
Mexico flagMexico·Clase I·I. Equipo Médico·AXMILAB, S.A. DE C.V.·Registered April 24, 2024
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
ABRA SMART BT.
Trade Name (English)
ABRA SMART BT.
Registration information
Analysis ID
1169E2024 SSA
Registration Date
April 24, 2024
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.
Name (English)
AXMILAB, S.A. DE C.V.
About this record

Access comprehensive regulatory information for DISPOSITIVO DE MONITOREO DE GLUCOSA EN SANGRE. (DISPOSITIVO DE MONITOREO DE GLUCOSA EN SANGRE.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1169E2024 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on April 24, 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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