76d5370e976af1d5fd8df7e163aaa562

1. ANTI-BRUCELLA ABORTUS ELISA (IGM)

BYO COLOMBIA S.A.S.·II·Colombia INVIMA·Expires September 01, 2033

Device classification

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

Registration information

Analysis ID: 76d5370e976af1d5fd8df7e163aaa562
Expire date: September 01, 2033

Authorized company / Fabricante

Name (Spanish): BYO COLOMBIA S.A.S.
Name (English): BYO 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 1. ANTI-BRUCELLA ABORTUS ELISA (IGM) (1. ANTI-BRUCELLA ABORTUS ELISA (IGM)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 76d5370e976af1d5fd8df7e163aaa562 and manufactured by BYO COLOMBIA S.A.S.. The device was registered on September 01, 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.