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CELLCHECK-400 - INVIMA Registration 229674b3085acc34bcdde1164ca72da2

Access comprehensive regulatory information for CELLCHECK-400 (CELLCHECK-400) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 229674b3085acc34bcdde1164ca72da2 and manufactured by SYSMEX COLOMBIA S.A.S. The device was registered on July 05, 2028.

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
229674b3085acc34bcdde1164ca72da2
CELLCHECK-400
INVIMA Analysis ID: 229674b3085acc34bcdde1164ca72da2
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N 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
229674b3085acc34bcdde1164ca72da2
Expire Date
July 05, 2028
Authorized Company / Fabricante
Name (Spanish)
SYSMEX COLOMBIA S.A.S
Name (English)
SYSMEX COLOMBIA S.A.S