DISPOSITIVO DE MONITOREO DE GLUCOSA EN SANGRE.
- 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.
- Analysis ID
- 1169E2024 SSA
- Registration Date
- April 24, 2024
- Name (Spanish)
- AXMILAB, S.A. DE C.V.
- Name (English)
- AXMILAB, S.A. DE C.V.
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.