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LIQUICHEK™ HEMATOLOGY CONTROL (A), TRILEVEL - INVIMA Registration ab377d2f3aa15cfa803072d4bf7e6718

Access comprehensive regulatory information for LIQUICHEK™ HEMATOLOGY CONTROL (A), TRILEVEL (LIQUICHEK™ HEMATOLOGY CONTROL (A), TRILEVEL) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID ab377d2f3aa15cfa803072d4bf7e6718 and manufactured by QUIK "QUALITY IS THE KEY" S.A.S.. The device was registered on May 31, 2033.

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
ab377d2f3aa15cfa803072d4bf7e6718
LIQUICHEK™ HEMATOLOGY CONTROL (A), TRILEVEL
INVIMA Analysis ID: ab377d2f3aa15cfa803072d4bf7e6718
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN 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
ab377d2f3aa15cfa803072d4bf7e6718
Expire Date
May 31, 2033
Authorized Company / Fabricante
Name (English)
QUIK "QUALITY IS THE KEY" S.A.S.