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REACTIVO DEL SISTEMA AUTOMÁTICO DE ANÁLISIS DE ORINA (EU-50) - INVIMA Registration a67e3beeb81e9863006b5a8d11d0d2b0

Access comprehensive regulatory information for REACTIVO DEL SISTEMA AUTOMÁTICO DE ANÁLISIS DE ORINA (EU-50) (AUTOMATIC URINALYSIS SYSTEM REAGENT (EU-50)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID a67e3beeb81e9863006b5a8d11d0d2b0 and manufactured by MINDRAY MEDICAL COLOMBIA S.A.S.. The device was registered on May 22, 2034.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
II
a67e3beeb81e9863006b5a8d11d0d2b0
REACTIVO DEL SISTEMA AUTOMÁTICO DE ANÁLISIS DE ORINA (EU-50)
INVIMA Analysis ID: a67e3beeb81e9863006b5a8d11d0d2b0
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Product Use / Uso del Producto
Spanish

SE UTILIZA PARA DILUIR MUESTRAS ANTES DEL ANÁLISIS _x000D_ DE ORINA Y LA PREPARACIÓN DE LA SUSPENSIÓN CELULAR.

English

USED TO DILUTE SAMPLES PRIOR TO ANALYSIS _x000D_ AND THE PREPARATION OF THE CELL SUSPENSION.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
a67e3beeb81e9863006b5a8d11d0d2b0
Expire Date
May 22, 2034
Authorized Company / Fabricante
Name (English)
MINDRAY MEDICAL COLOMBIA S.A.S.