Pure Global

EUROLINE ANTI-GANGLIOSIDES PROFILE 1 (IGG) - INVIMA Registration 0ac04d01d266887082b0aa6b700cc3b5

Access comprehensive regulatory information for EUROLINE ANTI-GANGLIOSIDES PROFILE 1 (IGG) (EUROLINE ANTI-GANGLIOSIDES PROFILE 1 (IGG)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 0ac04d01d266887082b0aa6b700cc3b5 and manufactured by BYO COLOMBIA SAS. The device was registered on January 03, 2031.

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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
II
0ac04d01d266887082b0aa6b700cc3b5
EUROLINE ANTI-GANGLIOSIDES PROFILE 1 (IGG)
INVIMA Analysis ID: 0ac04d01d266887082b0aa6b700cc3b5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

DETERMINACIร“N 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
0ac04d01d266887082b0aa6b700cc3b5
Expire Date
January 03, 2031
Authorized Company / Fabricante
Name (Spanish)
BYO COLOMBIA SAS
Name (English)
BYO COLOMBIA SAS