C.S.F. CONTROL LEVEL 2 & 3 (CSF CONTROL 2 & 3) - COFEPRIS Registration 1058R2018 SSA
Access comprehensive regulatory information for C.S.F. CONTROL LEVEL 2 & 3 (CSF CONTROL 2 & 3) (C.S.F. CONTROL LEVEL 2 & 3 (CSF CONTROL 2 & 3)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1058R2018 SSA and manufactured by SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.. The device was registered on May 03, 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 AL USO DE DIAGNÓSTICO IN VITRO, EN EL CONTROL DE CALIDAD DE LOS MÉTODOS DE DIAGNÓSTICO QUE UTILIZAN EL LCR COMO MUESTRA EN SISTEMAS DE QUÍMICA CLÍNICA. LOS CONTROLES CSF SON PARA EL CONTROL DE LA PRECISIÓN.
THIS PRODUCT IS INTENDED FOR USE IN VITRO DIAGNOSTICS, IN THE QUALITY CONTROL OF DIAGNOSTIC METHODS USING CSF AS A SAMPLE IN CLINICAL CHEMISTRY SYSTEMS. CSF CONTROLS ARE FOR PRECISION CONTROL.