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NORMA-IRP51 OP - INVIMA Registration 5f58490ce2f20d0058b3a59be0db0f2e

Access comprehensive regulatory information for NORMA-IRP51 OP (NORMA-IRP51 OP) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5f58490ce2f20d0058b3a59be0db0f2e and manufactured by LUMIRA S.A.S. The device was registered on November 14, 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
5f58490ce2f20d0058b3a59be0db0f2e
NORMA-IRP51 OP
INVIMA Analysis ID: 5f58490ce2f20d0058b3a59be0db0f2e
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
5f58490ce2f20d0058b3a59be0db0f2e
Expire Date
November 14, 2033
Authorized Company / Fabricante
Name (Spanish)
LUMIRA S.A.S
Name (English)
LUMIRA S.A.S