BIOMIC V3
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
- 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
- Analysis ID
- 1404E2019 SSA
- Registration Date
- July 19, 2019
- Name (Spanish)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
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.