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DENGUE IGG/IGM RAPID TEST - INVIMA Registration c1a89526fdf04d138570473fab07aa55

Access comprehensive regulatory information for DENGUE IGG/IGM RAPID TEST (DENGUE IGG/IGM RAPID TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID c1a89526fdf04d138570473fab07aa55 and manufactured by DIAGNOSTILAB VM SAS.

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
III
c1a89526fdf04d138570473fab07aa55
DENGUE IGG/IGM RAPID TEST
INVIMA Analysis ID: c1a89526fdf04d138570473fab07aa55
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Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
c1a89526fdf04d138570473fab07aa55
Authorized Company / Fabricante
Name (Spanish)
DIAGNOSTILAB VM SAS
Name (English)
DIAGNOSTILAB VM SAS