LIQUID IMMUNOASSAY CONTROL PREMIUM LEVEL 1, 2, 3 & TRI-LEVEL (LIQ IA PREMIUM 1, 2, 3 & TRI-LEVEL) - COFEPRIS Registration 704R2018 SSA
Access comprehensive regulatory information for LIQUID IMMUNOASSAY CONTROL PREMIUM LEVEL 1, 2, 3 & TRI-LEVEL (LIQ IA PREMIUM 1, 2, 3 & TRI-LEVEL) (LIQUID IMMUNOASSAY CONTROL PREMIUM LEVEL 1, 2, 3 & TRI-LEVEL (LIQ IA PREMIUM 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 704R2018 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.
LOS CONTROLES PARA INMUNOENSAYOS LÍQUIDOS PREMIUM DE RANDOX NIVEL 1, NIVEL 2, NIVEL 3 Y DE NIVEL TRIPLE SON CONTROLES LÍQUIDOS DESARROLLADOS PARA EL USO EN EL CONTROL DE CALIDAD DE ENSAYOS CUANTITATIVOS ESTIPULADOS EN EL INSERTO.
THE RANDOX LEVEL 1, LEVEL 2, LEVEL 3 AND TRIPLE LEVEL PREMIUM LIQUID IMMUNOASSAY CONTROLS ARE LIQUID CONTROLS DEVELOPED FOR USE IN THE QUALITY CONTROL OF QUANTITATIVE IN-INSERT ASSAYS.