VITROS TOXOPLASMA IGG - INVIMA Registration 539b441d974559a016e56665e571fde9
Access comprehensive regulatory information for VITROS TOXOPLASMA IGG (VITROS TOXOPLASMA IGG) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 539b441d974559a016e56665e571fde9 and manufactured by ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on March 15, 2031.
This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.
PARA LA DETERMINACION CUALITATIVA Y CUANTITATIVA DE ANTICUERPOS IGG FRENTE AL TOXOPLASMA GONDII EN SUERO Y PLASMA HUMANOS. UTILIZANDO EL SISTEMA DE INMUNODIAGNOSTICO VITROS ECI/ECIQ, EL SISTEMA DE INMUNODIAGNOSTICO VITROS 3600 Y EL SISTEMA INTEGRADO VITROS 5600 COMO AYUDA PARA EL DIAGNOSTICO DE INFECCION DE TOXOPLASMA GONDII.
FOR THE QUALITATIVE AND QUANTITATIVE DETERMINATION OF IGG ANTIBODIES AGAINST TOXOPLASMA GONDII IN HUMAN SERUM AND PLASMA. USING THE VITROS ECI/ECIQ IMMUNODIAGNOSTIC SYSTEM, THE VITROS 3600 IMMUNODIAGNOSTIC SYSTEM AND THE VITROS 5600 INTEGRATED SYSTEM AS AN AID FOR THE DIAGNOSIS OF TOXOPLASMA GONDII INFECTION.