BD VACUTAINER® BARRICOR™ LH PLASMA - COFEPRIS Registration 2733R2018 SSA
Access comprehensive regulatory information for BD VACUTAINER® BARRICOR™ LH PLASMA (BD VACUTAINER® BARRICOR™ LH PLASMA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2733R2018 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on December 10, 2018.
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.
LOS TUBOS BD VACUTAINER® BARRICOR™ LH PLASMA SON USADOS PARA RECOLECTAR, SEPARAR, PROCESAR, TRANSPORTAR Y ALMACENAR MUESTRAS DE SANGRE VENOSA PARA USO EN DETERMINACIONES QUÍMICAS, MONITOREO DE MEDICAMENTOS TERAPÉUTICOS, PRUEBAS DE DIAGNÓSTICO DE ENFERMEDA
BD VACUTAINER® BARRICOR™ LH PLASMA TUBES ARE USED TO COLLECT, SEPARATE, PROCESS, TRANSPORT AND STORE VENOUS BLOOD SAMPLES FOR USE IN CHEMICAL DETERMINATIONS, THERAPEUTIC DRUG MONITORING, DISEASE DIAGNOSTIC TESTS.