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FB - INVIMA Registration 788c2bc6603db9000b7ba480cedcb379

Access comprehensive regulatory information for FB (FB) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 788c2bc6603db9000b7ba480cedcb379 and manufactured by BIOMร‰RIEUX S.A. The device was registered on September 13, 2027.

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
788c2bc6603db9000b7ba480cedcb379
FB
INVIMA Analysis ID: 788c2bc6603db9000b7ba480cedcb379
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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
788c2bc6603db9000b7ba480cedcb379
Expire Date
September 13, 2027
Authorized Company / Fabricante
Name (Spanish)
BIOMร‰RIEUX S.A
Name (English)
BIOMร‰RIEUX S.A