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STANDARD™ F DENGUE NS1 AG FIA - INVIMA Registration e790df853002441b0d04391946056de1

Access comprehensive regulatory information for STANDARD™ F DENGUE NS1 AG FIA (STANDARD™ F DENGUE NS1 AG FIA) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID e790df853002441b0d04391946056de1 and manufactured by QUIMIOLAB S.A.S.

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
e790df853002441b0d04391946056de1
STANDARD™ F DENGUE NS1 AG FIA
INVIMA Analysis ID: e790df853002441b0d04391946056de1
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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
e790df853002441b0d04391946056de1
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S