4a9089d3cc8d9b8e057f7485bb53cf3c

IGE AU

BECKMAN COULTER COLOMBIA S.A.S.·II·Colombia INVIMA·Expires March 04, 2030

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 4a9089d3cc8d9b8e057f7485bb53cf3c
Expire date: March 04, 2030

Authorized company / Fabricante

Name (Spanish): BECKMAN COULTER COLOMBIA S.A.S.
Name (English): BECKMAN COULTER COLOMBIA S.A.S.

Product use / Uso del Producto

Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO._x000D_ _x000D_

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE ORGANISM HUMANO._x000D_ _x000D_

About this record

Access comprehensive regulatory information for IGE AU (IGE AU) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 4a9089d3cc8d9b8e057f7485bb53cf3c and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on March 04, 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.