ATELLICA IM SYPHILIS QUALITY CONTROL (SYPH QC) - INVIMA Registration d412484fd1a24bac2e5bc0e8b03e52ab
Access comprehensive regulatory information for ATELLICA IM SYPHILIS QUALITY CONTROL (SYPH QC) (ATELLICA IM SYPHILIS QUALITY CONTROL (SYPH QC)) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID d412484fd1a24bac2e5bc0e8b03e52ab and manufactured by SIEMENS HEALTHCARE S.A.S.. The device was registered on September 19, 2028.
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 ATELLICA IM SYPHILIS QUALITY CONTROL (SYPH QC)_x000D_ ESTÁ INDICADO PARA USO DIAGNÓSTICO IN VITRO EN LA _x000D_ MONITORIZACIÓN DE LOS RESULTADOS DEL ENSAYO _x000D_ ATELLICA IM SYPH CON EL USO DE UN ANALIZADOR DE _x000D_ INMUNOENSAYO ATELLICA.
THE ATELLICA IM SYPHILIS QUALITY CONTROL (SYPH QC)_x000D_ IT IS INDICATED FOR IN VITRO DIAGNOSTIC USE IN _x000D_ MONITORING THE RESULTS OF THE _x000D_ TRIAL ATELLICA IM SYPH WITH THE USE OF A _x000D_ ANALYZER ATELLICA IMMUNOASSAY.