UF II-REAGENTS - COFEPRIS Registration 2247R2019 SSA
Access comprehensive regulatory information for UF II-REAGENTS (UF II-REAGENTS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2247R2019 SSA and manufactured by SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.. The device was registered on December 12, 2019.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.
UF II REAGENTS ES EMPLEADO PARA LA DILUCIÓN DE ORINA Y CLASIFICACIÓN / RECUENTO DE BACTERIAS, EN ANALIZADOR DE PARTÍCULAS DE ORINA TOTALMENTE AUTOMATIZADO. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINE
UF II REAGENTS IS EMPLOYED FOR URINE DILUTION AND SORTING/COUNTING BACTERIA, IN FULLY AUTOMATED URINE PARTICLE ANALYZER. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE IN CLINICAL OR GABINE LABORATORIES ONLY.