IMMUNOASSAY CONTROL PREMIUM PLUS LEVEL 1, 2, 3 & TRI-LEVEL (IA PREMIUM PLUS 1, 2, 3 & TRI-LEVEL) - COFEPRIS Registration 703R2018 SSA
Access comprehensive regulatory information for IMMUNOASSAY CONTROL PREMIUM PLUS LEVEL 1, 2, 3 & TRI-LEVEL (IA PREMIUM PLUS 1, 2, 3 & TRI-LEVEL) (IMMUNOASSAY CONTROL PREMIUM PLUS LEVEL 1, 2, 3 & TRI-LEVEL (IA PREMIUM PLUS 1, 2, 3 & TRI-LEVEL)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 703R2018 SSA and manufactured by SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.. The device was registered on March 08, 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 DE DIAGNÓSTICO IN VITRO, COMO MATERIAL DE CONTROL DE CALIDAD ENSAYADO PARA MONITOREAR LA EXACTITUD Y REPRODUCIBILIDAD DE LOS ANALITOS ENLISTADOS EN EL INSERTO DEL EMPAQUE.AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCL
THIS PRODUCT IS INTENDED FOR IN VITRO DIAGNOSTIC USE, AS A QUALITY CONTROL MATERIAL TESTED TO MONITOR THE ACCURACY AND REPRODUCIBILITY OF THE ANALYTES LISTED ON THE PACKAGE INSERT. IN VITRO DIAGNOSTIC AGENT. FOR EXCL USE