aceac2b9113bba4dc239903aec47031f

IMMUNOGLOBULIN M REAGENT

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: aceac2b9113bba4dc239903aec47031f
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.

English

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

About this record

Access comprehensive regulatory information for IMMUNOGLOBULIN M REAGENT (IMMUNOGLOBULIN M REAGENT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID aceac2b9113bba4dc239903aec47031f 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.