Mexico COFEPRIS registration 721R2018 SSA

UF-CONTROL

EN: UF-CONTROL
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.·Registered March 08, 2018
Product Use / Uso del Producto
Spanish

EL UF-CONTROL ESTÁ INDICADO PARA VERIFICAR EL CORRECTO FUNCIONAMIENTO (CONTROL DE CALIDAD) DE LOS ANALIZADORES AUTOMATIZADOS DE PARTÍCULAS DE ORINA Y OTROS LÍQUIDOS CORPORALES SYSMEX. LOS PARÁMETROS DE CONTROL DE CALIDAD INCLUYEN ERITROCITOS “RBC ( /MCL)”

English

THE UF-CONTROL IS INDICATED TO VERIFY THE CORRECT OPERATION (QUALITY CONTROL) OF SYSMEX AUTOMATED ANALYZERS OF URINE PARTICLES AND OTHER BODY FLUIDS. QUALITY CONTROL PARAMETERS INCLUDE ERYTHROCYTES "RBC (/MCL)"

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
CONTROL PARA ANALIZADOR AUTOMATIZADO DE PARTÍCULAS DE ORINA Y OTROS LÍQUIDOS CORPORALES SYSMEX
Trade Name (English)
CONTROL FOR SYSMEX AUTOMATED ANALYZER OF URINE PARTICLES AND OTHER BODY FLUIDS
Registration information
Analysis ID
721R2018 SSA
Registration Date
March 08, 2018
Manufacturer / Fabricante
Name (English)
SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.
About this record

Access comprehensive regulatory information for UF-CONTROL (UF-CONTROL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 721R2018 SSA and manufactured by SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.. The device was registered on March 08, 2018.

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.

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