REVERSE DILUENT ORTHO BIOVUE SYSTEM (REVERSE DILUENT CASSETTE) - INVIMA Registration f81202df32d88b3f3f475b699691e473
Access comprehensive regulatory information for REVERSE DILUENT ORTHO BIOVUE SYSTEM (REVERSE DILUENT CASSETTE) (REVERSE DILUENT ORTHO BIOVUE SYSTEM (REVERSE DILUENT CASSETTE)) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID f81202df32d88b3f3f475b699691e473 and manufactured by ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on June 11, 2029.
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 USO DIAGNÓSTICO IN VITRO. PRINCIPALMENTE, PARA_x000D_ DETERMINACIÓN DE LOS ANTICUERPOS ESPERADOS DEL _x000D_ GRUPO SANGUÍNEO ABO Y PARA PROCEDIMIENTOS DE _x000D_ CRIBADO DE ANTICUERPOS PARA LA AGLUTINACIÓN _x000D_ DIRECTA.
FOR IN VITRO DIAGNOSTIC USE. MAINLY, PARA_x000D_ DETERMINATION OF EXPECTED ANTIBODIES FROM THE _x000D_ ABO BLOOD TYPE AND FOR _x000D_ PROCEDURES ANTIBODY SCREENING FOR _x000D_ CLUMPING DIRECT.