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ACE - INVIMA Registration 3e24264cf6b8d22f256ee46138bf4f7e

Access comprehensive regulatory information for ACE (ACE) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 3e24264cf6b8d22f256ee46138bf4f7e and manufactured by QUIK "QUALITY IS THE KEY" S.A.S.. The device was registered on July 14, 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
3e24264cf6b8d22f256ee46138bf4f7e
ACE
INVIMA Analysis ID: 3e24264cf6b8d22f256ee46138bf4f7e
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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
3e24264cf6b8d22f256ee46138bf4f7e
Expire Date
July 14, 2032
Authorized Company / Fabricante
Name (English)
QUIK "QUALITY IS THE KEY" S.A.S.