NEO IRIS™ - COFEPRIS Registration 1881E2019 SSA
Access comprehensive regulatory information for NEO IRIS™ (NEO IRIS™) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1881E2019 SSA and manufactured by LABORATORIOS LICON, S.A.. The device was registered on September 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.
NEO IRIS ES UN INSTRUMENTO CONTROLADO POR MICROPROCESADORES DISEÑADO PARA AUTOMATIZAR COMPLETAMENTE LAS PRUEBAS DIAGNÓSTICAS IN VITRO DE INMUNOHEMATOLOGÍA DE SANGRE HUMANA. AUTOMATIZA LAS FUNCIONES DE ADMINISTRACIÓN DE DATOS, INTERPRETACIÓN DE RESULTADOS
NEO IRIS IS A MICROPROCESSOR-CONTROLLED INSTRUMENT DESIGNED TO FULLY AUTOMATE IN VITRO DIAGNOSTIC TESTING OF HUMAN BLOOD IMMUNOHEMATOLOGY. AUTOMATES DATA MANAGEMENT FUNCTIONS, INTERPRETATION OF RESULTS