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PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS - COFEPRIS Registration 1855R2024 SSA

Access comprehensive regulatory information for PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS (PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1855R2024 SSA and manufactured by DRPRO MED S.A. DE C.V.. The device was registered on July 02, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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
1855R2024 SSA
PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS
COFEPRIS Analysis ID: 1855R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
D-DIMER (CLIA) - WONDFO
Trade Name (English)
D-DIMER (CLIA) - WONDFO
Registration Information
Analysis ID
1855R2024 SSA
Registration Date
July 02, 2024
Manufacturer / Fabricante
Name (English)
DRPRO MED S.A. DE C.V.