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CK-MB, LIQUID - INVIMA Registration b5964314eb5468341e3a73bc1fd09808

Access comprehensive regulatory information for CK-MB, LIQUID (CK-MB, LIQUID) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b5964314eb5468341e3a73bc1fd09808 and manufactured by QUIK "QUALITY IS THE KEY" S.A.S.. The device was registered on September 05, 2032.

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
b5964314eb5468341e3a73bc1fd09808
CK-MB, LIQUID
INVIMA Analysis ID: b5964314eb5468341e3a73bc1fd09808
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b5964314eb5468341e3a73bc1fd09808
Expire Date
September 05, 2032
Authorized Company / Fabricante
Name (English)
QUIK "QUALITY IS THE KEY" S.A.S.