Mexico COFEPRIS registration 1602E2022 SSA
GLUCÓMETRO
EN: GLUCÓMETRO
Mexico·Clase II·I. Equipo Médico·ABBOTT
LABORATORIES DE
MÉXICO, S.A. DE C.V.·Registered December 15, 2022Device 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.
About this record
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.
Free DatabasePowered by Pure Global AICOFEPRIS Official DataClase II