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GELOSE PYLORI / PYLORI AGAR - INVIMA Registration a365797ae9c8694801a26376f9abeddd

Access comprehensive regulatory information for GELOSE PYLORI / PYLORI AGAR (GELOSE PYLORI / PYLORI AGAR ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID a365797ae9c8694801a26376f9abeddd and manufactured by BIOMร‰RIEUX S.A. The device was registered on February 28, 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.

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INVIMA Official Data
I
a365797ae9c8694801a26376f9abeddd
GELOSE PYLORI / PYLORI AGAR
INVIMA Analysis ID: a365797ae9c8694801a26376f9abeddd
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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
I
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
a365797ae9c8694801a26376f9abeddd
Expire Date
February 28, 2030
Authorized Company / Fabricante
Name (Spanish)
BIOMร‰RIEUX S.A
Name (English)
BIOMร‰RIEUX S.A