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GELOSE CHROMID SALMONELLA ELITE / CHROMID SALMONELLA ELITE AGAR - INVIMA Registration 71b105f5756cd5342192e5007e183c86

Access comprehensive regulatory information for GELOSE CHROMID SALMONELLA ELITE / CHROMID SALMONELLA ELITE AGAR (GELOSE CHROMID SALMONELLA ELITE / CHROMID SALMONELLA ELITE AGAR) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 71b105f5756cd5342192e5007e183c86 and manufactured by BIOMร‰RIEUX S.A. The device was registered on August 27, 2028.

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
71b105f5756cd5342192e5007e183c86
GELOSE CHROMID SALMONELLA ELITE / CHROMID SALMONELLA ELITE AGAR
INVIMA Analysis ID: 71b105f5756cd5342192e5007e183c86
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO _x000D_ _x000D_

English

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

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
71b105f5756cd5342192e5007e183c86
Expire Date
August 27, 2028
Authorized Company / Fabricante
Name (Spanish)
BIOMร‰RIEUX S.A
Name (English)
BIOMร‰RIEUX S.A