STANDARD™ C.DIFFICILE TOXIN AB CONTROL - INVIMA Registration 490f9d04f1226af80b8645987c2a5109
Access comprehensive regulatory information for STANDARD™ C.DIFFICILE TOXIN AB CONTROL (STANDARD™ C.DIFFICILE TOXIN AB CONTROL) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 490f9d04f1226af80b8645987c2a5109 and manufactured by QUIMIOLAB S.A.S. The device was registered on June 11, 2034.
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.
EL PRODUCTO STANDARD C. DIFFICILE TOXIN A/B CONTROL HA SIDO DESARROLLADO PARA EMPLEARSE _x000D_ COMO MATERIAL DE CONTROL DE CALIDAD EXTERNO PARA MONITOREAR EL DESEMPEÑO DE LAS _x000D_ PRUEBAS STANDARD F C. DIFFICILE TOXIN A/B FIA. ES IMPORTANTE DESARROLLAR PRUEBAS _x000D_ DE CONTROL CON MATERIALES DE CONTROL POSITIVO Y NEGATIVO PARA ASEGURAR EL CORRECTO _x000D_ FUNCIONAMIENTO DEL SISTEMA QUE USTED HA ELEGIDO
THE STANDARD PRODUCT C. DIFFICILE TOXIN A/B CONTROL HAS BEEN DEVELOPED FOR USE _x000D_ AS AN EXTERNAL QUALITY CONTROL MATERIAL TO MONITOR THE PERFORMANCE OF _x000D_ STANDARD F C. DIFFICILE TOXIN A/B FIA TESTS. IT IS IMPORTANT TO DEVELOP _x000D_ TESTS WITH POSITIVE AND NEGATIVE CONTROL MATERIALS TO ENSURE THE CORRECT _x000D_ OPERATION OF THE SYSTEM YOU HAVE CHOSEN