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AQT 90 FLEX SOLUTION PACK - INVIMA Registration 50bcf970eff263e274cafd8f9eedea5f

Access comprehensive regulatory information for AQT 90 FLEX SOLUTION PACK (AQT 90 FLEX SOLUTION PACK) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 50bcf970eff263e274cafd8f9eedea5f and manufactured by INSTRUMENTACION S.A.. The device was registered on March 19, 2031.

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
50bcf970eff263e274cafd8f9eedea5f
AQT 90 FLEX SOLUTION PACK
INVIMA Analysis ID: 50bcf970eff263e274cafd8f9eedea5f
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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
50bcf970eff263e274cafd8f9eedea5f
Expire Date
March 19, 2031
Authorized Company / Fabricante
Name (Spanish)
INSTRUMENTACION S.A.
Name (English)
INSTRUMENTACION S.A.