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VITEK 2 AST-N401 - INVIMA Registration 6895e10d0fadca82ab8625ea6db2ebb1

Access comprehensive regulatory information for VITEK 2 AST-N401 (VITEK 2 AST-N401) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 6895e10d0fadca82ab8625ea6db2ebb1 and manufactured by BIOMร‰RIEUX S.A. The device was registered on November 27, 2030.

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
6895e10d0fadca82ab8625ea6db2ebb1
VITEK 2 AST-N401
INVIMA Analysis ID: 6895e10d0fadca82ab8625ea6db2ebb1
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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
6895e10d0fadca82ab8625ea6db2ebb1
Expire Date
November 27, 2030
Authorized Company / Fabricante
Name (Spanish)
BIOMร‰RIEUX S.A
Name (English)
BIOMร‰RIEUX S.A