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1. ELUENT A - INVIMA Registration 06181499599bbf610ec07141edbf4534

Access comprehensive regulatory information for 1. ELUENT A (1. ELECTED A) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 06181499599bbf610ec07141edbf4534 and manufactured by DIAGNOSTILAB VM SAS. The device was registered on August 24, 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
06181499599bbf610ec07141edbf4534
1. ELUENT A
INVIMA Analysis ID: 06181499599bbf610ec07141edbf4534
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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
06181499599bbf610ec07141edbf4534
Expire Date
August 24, 2033
Authorized Company / Fabricante
Name (Spanish)
DIAGNOSTILAB VM SAS
Name (English)
DIAGNOSTILAB VM SAS