GLUCÓMETRO - COFEPRIS Registration 1602E2022 SSA
Access comprehensive regulatory information for GLUCÓMETRO (GLUCÓMETRO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1602E2022 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on December 15, 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 II
1602E2022 SSA
GLUCÓMETRO
COFEPRIS Analysis ID: 1602E2022 SSA
Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
LECTOR FREESTYLE LIBRE
SISTEMA FLASH DE MONITOREO
DE GLUCOSA
Trade Name (English)
LECTOR FREESTYLE LIBRE
SISTEMA FLASH DE MONITOREO
DE GLUCOSA
Registration Information
Analysis ID
1602E2022 SSA
Registration Date
December 15, 2022
Manufacturer / Fabricante
Name (Spanish)
ABBOTT
LABORATORIES DE
MÉXICO, S.A. DE C.V.Name (English)
ABBOTT
LABORATORIES DE
MÉXICO, S.A. DE C.V.