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CYFLOW™ CD13 PE-CY7 - INVIMA Registration 8b8eac2dc2a95f024117e7c4b188399b

Access comprehensive regulatory information for CYFLOW™ CD13 PE-CY7 (CYFLOW™ CD13 PE-CY7) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 8b8eac2dc2a95f024117e7c4b188399b and manufactured by SYSMEX COLOMBIA SAS. The device was registered on November 24, 2030.

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
8b8eac2dc2a95f024117e7c4b188399b
CYFLOW™ CD13 PE-CY7
INVIMA Analysis ID: 8b8eac2dc2a95f024117e7c4b188399b
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
8b8eac2dc2a95f024117e7c4b188399b
Expire Date
November 24, 2030
Authorized Company / Fabricante
Name (Spanish)
SYSMEX COLOMBIA SAS
Name (English)
SYSMEX COLOMBIA SAS