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1. 449 LIQUICHEK ? HEMATOLOGY CONTROL (S) LEVEL 1,2 AND 3 - INVIMA Registration 2154d9fd42f904468f1a81f18b2857ab

Access comprehensive regulatory information for 1. 449 LIQUICHEK ? HEMATOLOGY CONTROL (S) LEVEL 1,2 AND 3 (1. 449 LIQUICHEK ? HEMATOLOGY CONTROL (S) LEVEL 1,2 AND 3) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 2154d9fd42f904468f1a81f18b2857ab and manufactured by QUIK "QUALITY IS THE KEY" S.A.S.. The device was registered on January 12, 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
2154d9fd42f904468f1a81f18b2857ab
1. 449 LIQUICHEK ? HEMATOLOGY CONTROL (S) LEVEL 1,2 AND 3
INVIMA Analysis ID: 2154d9fd42f904468f1a81f18b2857ab
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Product Use / Uso del Producto
Spanish

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

English

DETERMINATION OF 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
2154d9fd42f904468f1a81f18b2857ab
Expire Date
January 12, 2032
Authorized Company / Fabricante
Name (English)
QUIK "QUALITY IS THE KEY" S.A.S.