6dbe1d2c61b155462de5e9c5aa630e63

4. CYTOKINE STORM ARRAY CONTROL KIT MARCA: RANDOX

BIOLORE LTDA·I·Colombia INVIMA·Expires February 22, 2034

Device classification

Risk class / Clase de Riesgo: I
Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: 6dbe1d2c61b155462de5e9c5aa630e63
Expire date: February 22, 2034

Authorized company / Fabricante

Name (Spanish): BIOLORE LTDA
Name (English): BIOLORE LTDA

Product use / Uso del Producto

Spanish

LOS CONTROLES RANDOX EVIDENCE MULTISTAT CYTOKINE STORM ARRAY ESTÁN DISEÑADOS PARA USARSE COMO CONTROL DE CALIDAD ANALIZADO EN LA RUTINA._x000D_ MONITOREO DE LA EXACTITUD Y PRECISIÓN DE LOS ANALITOS ENUMERADOS EN ESTE PROSPECTO._x000D_ LOS CONTROLES RANDOX EVIDENCE MULTISTAT CYTOKINE STORM ARRAY SON MULTIANALITOS Y CONTIENEN IL-1BETA, IL-2, IL-6, IL-15,_x000D_ IFNGAMMA, TNFALFA, MCP-1, FERRITINA Y DÍMERO D. HAY DOS NIVELES DE CONTROL: BAJO Y ALTO CORRESPONDIENTES AL NIVEL 1 Y AL NIVEL 2_x000D_ RESPECTIVAMENTE

English

THE RANDOX EVIDENCE MULTISTAT CYTOKINE STORM ARRAY CONTROLS ARE DESIGNED TO BE USED AS AN ANALYZED QUALITY CONTROL IN THE RUTINA._x000D_ MONITORING THE ACCURACY AND PRECISION OF THE ANALYTES LISTED IN THIS PROSPECTO._x000D_ THE RANDOX EVIDENCE MULTISTAT CYTOKINE STORM ARRAY CONTROLS ARE MULTIANALYTES AND CONTAIN IL-1BETA, IL-2, IL-6, IL-15,_x000D_ IFNGAMMA, TNFALFA, MCP-1, FERRITIN, AND DIMER D. THERE ARE TWO LEVELS OF CONTROL: LOW AND HIGH CORRESPONDING TO LEVEL 1 AND LEVEL 2_x000D_ RESPECTIVELY

About this record

Access comprehensive regulatory information for 4. CYTOKINE STORM ARRAY CONTROL KIT MARCA: RANDOX (4. CYTOKINE STORM ARRAY CONTROL KIT MARCA: RANDOX) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 6dbe1d2c61b155462de5e9c5aa630e63 and manufactured by BIOLORE LTDA. The device was registered on February 22, 2034.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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.