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FERRITIN - INVIMA Registration da6074e9a14abd1b134ce106eb507b36

Access comprehensive regulatory information for FERRITIN (FERRITIN) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID da6074e9a14abd1b134ce106eb507b36 and manufactured by BECKMAN COULTER COLOMBIA S.A.S. The device was registered on June 21, 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
II
da6074e9a14abd1b134ce106eb507b36
FERRITIN
INVIMA Analysis ID: da6074e9a14abd1b134ce106eb507b36
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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
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
da6074e9a14abd1b134ce106eb507b36
Expire Date
June 21, 2027
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA S.A.S