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R EXTEM® - INVIMA Registration 4fde090388394f5db15bdb9f1533505e

Access comprehensive regulatory information for R EXTEM® (R EXTEM® ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 4fde090388394f5db15bdb9f1533505e and manufactured by WERFEN COLOMBIA SAS. The device was registered on December 20, 2027.

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
4fde090388394f5db15bdb9f1533505e
R EXTEM®
INVIMA Analysis ID: 4fde090388394f5db15bdb9f1533505e
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN 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
4fde090388394f5db15bdb9f1533505e
Expire Date
December 20, 2027
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA SAS
Name (English)
THROW COLOMBIA SAS