096562734ae03d1066a016c464c5c3c1

LUMI-PHOS PRO

BECKMAN COULTER COLOMBIA S.A.S.·II·Colombia INVIMA·Expires March 24, 2033

Device classification

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

Registration information

Analysis ID: 096562734ae03d1066a016c464c5c3c1
Expire date: March 24, 2033

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_x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALITOS_x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM

About this record

Access comprehensive regulatory information for LUMI-PHOS PRO (LUMI-PHOS PRO) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 096562734ae03d1066a016c464c5c3c1 and manufactured by BECKMAN COULTER COLOMBIA S.A.S.. The device was registered on March 24, 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.