STANDARD™ F C.DIFFICILE TOXIN AB FIA - INVIMA Registration 7d41583375ba6639e61b88583d308dcb
Access comprehensive regulatory information for STANDARD™ F C.DIFFICILE TOXIN AB FIA (STANDARD™ F C.DIFFICILE TOXIN AB FIA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 7d41583375ba6639e61b88583d308dcb 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.
LA PRUEBA STANDARD F C. DIFFICILE TOXIN A/B FIA ES PARA MEDIR CUALITATIVAMENTE LA _x000D_ TOXINA C. DIFFICILE A/B EN DIAGNÓSTICO IN VITRO. ESTE PRODUCTO ES ÚNICAMENTE PARA USO _x000D_ PROFESIONAL Y OTORGA SÓLO UN RESULTADO DE CONTROL INICIAL. LA PRUEBA STANDARD F C. _x000D_ DIFFICILE TOXIN A/B FIA DEBE SER UTILIZADA CON EL ANALIZADOR ADECUADO, ANALIZADORES _x000D_ STANDARD F, FABRICADOS POR SD BIOSENSOR.
THE STANDARD F C. DIFFICILE TOXIN A/B FIA TEST IS FOR QUALITATIVELY MEASURING _x000D_ C. DIFFICILE TOXIN A/B IN VITRO DIAGNOSIS. THIS PRODUCT IS FOR _x000D_ USE ONLY PROFESSIONAL AND GIVES ONLY AN INITIAL CONTROL RESULT. THE STANDARD TEST F C. _x000D_ DIFFICILE TOXIN A/B FIA SHOULD BE USED WITH THE RIGHT ANALYZER, ANALYZERS, _x000D_ STANDARD F, MANUFACTURED BY SD BIOSENSOR.