ANTI-IGM. - COFEPRIS Registration 1808R2019 SSA
Access comprehensive regulatory information for ANTI-IGM. (ANTI-IGM.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1808R2019 SSA and manufactured by BIO-RAD, S.A.. The device was registered on September 03, 2019.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
EL PRESENTE TEST SIRVE PARA LA DETERMINACIÓN Y LA IDENTIFICACIÓN DE ANTICUERPOS, ASÍ COMO PARA DETERMINAR LA COMPATIBILIDAD (TEST CRUZADO). SE EMPLEAN PARA DETERMINAR LOS ANTICUERPOS DE LAS CORRESPONDIENTES CLASES DE INMUNOGLOBULINA UNIDOS A LOS ERITROC
THIS TEST IS USED FOR THE DETERMINATION AND IDENTIFICATION OF ANTIBODIES, AS WELL AS TO DETERMINE COMPATIBILITY (CROSS-OVER TEST). THEY ARE USED TO DETERMINE THE ANTIBODIES OF THE CORRESPONDING CLASSES OF IMMUNOGLOBULIN ATTACHED TO ERYTHROC