BATROXOBIN REAGENT - INVIMA Registration 0e39f4aa1397783a187198d9f885e718
Access comprehensive regulatory information for BATROXOBIN REAGENT (BATROXOBIN REAGENT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 0e39f4aa1397783a187198d9f885e718 and manufactured by SIEMENS HEALTHCARE S.A.S. The device was registered on January 29, 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.
BATROXOBIN REAGENT ES UN REACTIVO DE DIAGNÓSTICO IN VITRO QUE SE USA PARA LA DETERMINACIÓN_x000D_ CUANTITATIVA DEL TIEMPO DE BATROXOBINA COMO AYUDA EN EL DIAGNÓSTICO DE TRASTORNOS DE LA HEMOSTASIA_x000D_ RELACIONADOS CON EL FIBRINÓGENO EN PACIENTES QUE SUFREN, O CON RIESGO DE SUFRIR, TRASTORNOS_x000D_ HEMORRÁGICOS EN PLASMA HUMANO CON CITRATO SÓDICO MEDIANTE MÉTODOS COAGULOMÉTRICOS_x000D_ AUTOMATIZADOS, SEMIAUTOMATIZADOS Y/O MANUALES._x000D_ PARA LAS PRUEBAS DEL TIEMPO DE BATROXOBINA NO EXISTE NINGÚN PREPARADO NI MÉTODO DE REFERENCIA_x000D_ INTERNACIONAL.
BATROXOBIN REAGENT IS AN IN VITRO DIAGNOSTIC REAGENT USED FOR DETERMINACIÓN_x000D_ QUANTITATIVE TIME ASSESSMENT OF BATROXOBIN AS AN AID IN THE DIAGNOSIS OF HEMOSTASIA_x000D_ DISORDERS FIBRINOGEN-RELATED IN PATIENTS SUFFERING FROM, OR AT RISK OF, TRASTORNOS_x000D_ HEMORRHAGIC CASES IN HUMAN PLASMA WITH SODIUM CITRATE USING COAGULOMÉTRICOS_x000D_ METHODS AUTOMATED, SEMI-AUTOMATED AND/OR MANUALES._x000D_ THERE IS NO PREPARATION OR METHOD OF REFERENCIA_x000D_ FOR BATROXOBIN TIME TESTS INTERNATIONAL.