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FERRITIN (CLIA) - INVIMA Registration 37a469be07efd7168ce1b17ff2edec73

Access comprehensive regulatory information for FERRITIN (CLIA) (FERRITIN (CLIA)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 37a469be07efd7168ce1b17ff2edec73 and manufactured by LUMIRA S.A.S. The device was registered on December 27, 2032.

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
37a469be07efd7168ce1b17ff2edec73
FERRITIN (CLIA)
INVIMA Analysis ID: 37a469be07efd7168ce1b17ff2edec73
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS_x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL_x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALITOS_x000D_ RELATED TO SAMPLES FROM DEL_x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
37a469be07efd7168ce1b17ff2edec73
Expire Date
December 27, 2032
Authorized Company / Fabricante
Name (Spanish)
LUMIRA S.A.S
Name (English)
LUMIRA S.A.S