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ANALIZADORES DE HEMOGLOBIMA GLICOSILADA - COFEPRIS Registration 1740E2024 SSA

Access comprehensive regulatory information for ANALIZADORES DE HEMOGLOBIMA GLICOSILADA (ANALIZADORES DE HEMOGLOBIMA GLICOSILADA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1740E2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on June 20, 2024.

This page provides complete registration details including product type (I. Equipo Mรฉdico), 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 I
1740E2024 SSA
ANALIZADORES DE HEMOGLOBIMA GLICOSILADA
COFEPRIS Analysis ID: 1740E2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. Equipo Mรฉdico
Product Type (English)
I. Equipo Mรฉdico
Trade Name (Spanish)
LIFOTRONIC HBA1C ANALYZER
Trade Name (English)
LIFOTRONIC HBA1C ANALYZER
Registration Information
Analysis ID
1740E2024 SSA
Registration Date
June 20, 2024
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.