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LIQUICHEK™ HEMATOLOGY CONTROL (C) LOW, NORMAL AND HIGH - INVIMA Registration eb1ff6d92e34b6c274ada6a756faf16b

Access comprehensive regulatory information for LIQUICHEK™ HEMATOLOGY CONTROL (C) LOW, NORMAL AND HIGH (LIQUICHEK™ HEMATOLOGY CONTROL (C) LOW, NORMAL AND HIGH) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID eb1ff6d92e34b6c274ada6a756faf16b and manufactured by QUIK "QUALITY IS THE KEY" S.A.S.. The device was registered on March 01, 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
eb1ff6d92e34b6c274ada6a756faf16b
LIQUICHEK™ HEMATOLOGY CONTROL (C) LOW, NORMAL AND HIGH
INVIMA Analysis ID: eb1ff6d92e34b6c274ada6a756faf16b
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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
eb1ff6d92e34b6c274ada6a756faf16b
Expire Date
March 01, 2033
Authorized Company / Fabricante
Name (English)
QUIK "QUALITY IS THE KEY" S.A.S.