Mexico COFEPRIS registration 0319E2024 SSA
GLÚCOMETRO
EN: GLÚCOMETRO
Mexico·Clase I·I. Equipo Médico·AXMILAB, S.A. DE C.V.·Registered January 30, 2024Device 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.
About this record
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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