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CARESENS PRO - COFEPRIS Registration 511R2022 SSA

Access comprehensive regulatory information for CARESENS PRO (CARESENS PRO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 511R2022 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on June 17, 2022.

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 I
511R2022 SSA
CARESENS PRO
COFEPRIS Analysis ID: 511R2022 SSA
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Product Use / Uso del Producto
Spanish

TIRA REACTIVA Y SOLUCIÓN CONTROL PARA LADETERMINACIÓN DE GLUCOSA EN SANGRE

English

TEST STRIP AND CONTROL SOLUTION FOR BLOOD GLUCOSE DETERMINATION

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
TIRA REACTIVA Y SOLUCIÓNCONTROL PARA LADETERMINACIÓN DEGLUCOSAEN SANGRE
Trade Name (English)
TEST STRIP AND CONTROL SOLUTION FOR BLOOD GLUCOSE DETERMINATION
Registration Information
Analysis ID
511R2022 SSA
Registration Date
June 17, 2022
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.
Name (English)
AXMILAB, S.A. DE C.V.