CARLOS DE SOUZA, J.; MEHRPOUR, S.; MODOLO FERREIRA, M.; LUDUVICO COELHO, Y. .; DE CASTRO VIVAS, G.; DELISLE RODRIGUEZ, D.; DE ASSIS SANTOS, F.; FREIRE BASTOS-FILHO, T. Evaluation of Adverse Events Recorded in FDA/USA and ANVISA/Brazil Databases for Medical Devices: Defibrillator, Infusion Pump, Physiological Monitor, Pulmonary Ventilator and Ultrasonic Scalpel. Global Clinical Engineering Journal, [S. l.], v. 4, n. 2, p. 5–14, 2021. DOI: 10.31354/globalce.v4i2.121. Disponível em: Acesso em: 28 nov. 2021.