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1. NORMA-IRP20 - INVIMA Registration 5c65b81107b5d50b177a8ce8053ac2cf

Access comprehensive regulatory information for 1. NORMA-IRP20 (1. STANDARD-IRP20) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5c65b81107b5d50b177a8ce8053ac2cf and manufactured by LUMIRA S.A.S. The device was registered on April 09, 2034.

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
5c65b81107b5d50b177a8ce8053ac2cf
1. NORMA-IRP20
INVIMA Analysis ID: 5c65b81107b5d50b177a8ce8053ac2cf
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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
5c65b81107b5d50b177a8ce8053ac2cf
Expire Date
April 09, 2034
Authorized Company / Fabricante
Name (Spanish)
LUMIRA S.A.S
Name (English)
LUMIRA S.A.S