Mexico COFEPRIS registration 1404E2019 SSA

BIOMIC V3

EN: BIOMIC V3
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·BECTON DICKINSON DE MÉXICO, S.A. DE C.V.·Registered July 19, 2019
Product Use / Uso del Producto
Spanish

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

English

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

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
LECTOR DE PLACAS Y/O PANELES PARA PRUEBAS MICROBIOLÓGICAS
Trade Name (English)
PLATE AND/OR PANEL READER FOR MICROBIOLOGICAL TESTING
Registration information
Analysis ID
1404E2019 SSA
Registration Date
July 19, 2019
Manufacturer / Fabricante
Name (English)
BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
About this record

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.

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