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BODITECH DENGUE IGG/IGM CONTROL_x000D_ - INVIMA Registration a112647a0ad1d50caec3de3c79d612a8

Access comprehensive regulatory information for BODITECH DENGUE IGG/IGM CONTROL_x000D_ (BODITECH DENGUE IGG/IGM CONTROL_x000D_) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID a112647a0ad1d50caec3de3c79d612a8 and manufactured by ANNAR DIAGNOSTICA IMPORT 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
a112647a0ad1d50caec3de3c79d612a8
BODITECH DENGUE IGG/IGM CONTROL_x000D_
INVIMA Analysis ID: a112647a0ad1d50caec3de3c79d612a8
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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
a112647a0ad1d50caec3de3c79d612a8
Authorized Company / Fabricante
Name (English)
ANNAR DIAGNOSTICA IMPORT S.A.S.