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GLUCOA1C KIT DE PRUEBA DE GLICOHEMOGLOBINA - COFEPRIS Registration 640R2019 SSA

Access comprehensive regulatory information for GLUCOA1C KIT DE PRUEBA DE GLICOHEMOGLOBINA (GLUCOA1C GLYCOHEMOGLOBIN TEST KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 640R2019 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on March 27, 2019.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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
640R2019 SSA
GLUCOA1C KIT DE PRUEBA DE GLICOHEMOGLOBINA
COFEPRIS Analysis ID: 640R2019 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA MEDICIร“N CUANTITATIVA DEL NIVEL DE HEMOGLOBINA (HBA1C) EN MUESTRAS DE SANGRE TOTAL (SANGRE CAPILAR O VENOSA)

English

QUANTITATIVE HEMOGLOBIN LEVEL MEASUREMENT TEST (HBA1C) IN WHOLE BLOOD SAMPLES (CAPILLARY OR VENOUS BLOOD)

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
PRUEBA MEDICIร“N CUANTITATIVA DEL NIVEL DE HEMOGLOBINA (HBA1C) EN MUESTRAS DE SANGRE TOTAL (SANGRE CA
Trade Name (English)
QUANTITATIVE HEMOGLOBIN LEVEL MEASUREMENT TEST (HBA1C) IN WHOLE BLOOD SAMPLES (CA BLOOD
Registration Information
Analysis ID
640R2019 SSA
Registration Date
March 27, 2019
Manufacturer / Fabricante
Name (English)
KANA UNDESA, S.A. DE C.V.