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CMD 600 REAGENT MODULE HT Y LT. - COFEPRIS Registration 2014R2019 SSA

Access comprehensive regulatory information for CMD 600 REAGENT MODULE HT Y LT. (CMD 600 REAGENT MODULE HT Y LT.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2014R2019 SSA and manufactured by REPRESENTACIONES LABIN Mร‰XICO, S.A. DE C.V.. The device was registered on October 18, 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 I
2014R2019 SSA
CMD 600 REAGENT MODULE HT Y LT.
COFEPRIS Analysis ID: 2014R2019 SSA
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Product Use / Uso del Producto
Spanish

CALIBRADOR PARA USO EN EL EQUIPO DE QUรMICA CLรNICA.

English

CALIBRATOR FOR USE IN CLINICAL CHEMISTRY EQUIPMENT.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO CALIBRADOR.
Trade Name (English)
CALIBRATOR REAGENT.
Registration Information
Analysis ID
2014R2019 SSA
Registration Date
October 18, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTACIONES LABIN Mร‰XICO, S.A. DE C.V.