BIOMIC V3 - COFEPRIS Registration 1404E2019 SSA
Access comprehensive regulatory information for BIOMIC V3 (BIOMIC V3) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1404E2019 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on July 19, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 DISPOSITIVO BIOMIC® V3 ES UTILIZADO PARA REALIZAR LECTURA AUTOMATIZADA, FACILITAR LA INTERPRETACIÓN, ESTANDARIZACIÓN, REGISTRO Y REPORTE DE LOS RESULTADOS DE PRUEBAS MICROBIOLÓGICAS COMO SON LAS PRUEBAS DE SUSCEPTIBILIDAD ANTIMICROBIANA, IDENTIFICACIÓN
THE BIOMIC® V3 DEVICE IS USED TO PERFORM AUTOMATED READING, FACILITATE THE INTERPRETATION, STANDARDIZATION, RECORDING AND REPORTING OF MICROBIOLOGICAL TEST RESULTS SUCH AS ANTIMICROBIAL SUSCEPTIBILITY TESTS, IDENTIFICATION