TRI-LEVEL CARDIAC CONTROL (CRD CONTROL) - COFEPRIS Registration 1947R2018 SSA
Access comprehensive regulatory information for TRI-LEVEL CARDIAC CONTROL (CRD CONTROL) (TRI-LEVEL CARDIAC CONTROL (CRD CONTROL)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1947R2018 SSA and manufactured by SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.. The device was registered on August 07, 2018.
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.
ESTE PRODUCTO ESTÁ DESTINADO PARA USO DIAGNÓSTICO IN VITRO, EN EL CONTROL DE CALIDAD DE MARCADORES CARDÍACOS EN QUÍMICA CLÍNICA Y SISTEMAS DE INMUNOENSAYO.
THIS PRODUCT IS INTENDED FOR IN VITRO DIAGNOSTIC USE, IN THE QUALITY CONTROL OF CARDIAC MARKERS IN CLINICAL CHEMISTRY AND IMMUNOASSAY SYSTEMS.