STANDARD™ Q CHIKUNGUNYA IGM/IGG TEST - INVIMA Registration 1ef8ec7d8a8b7c34dd02408bd7ebfa04
Access comprehensive regulatory information for STANDARD™ Q CHIKUNGUNYA IGM/IGG TEST (STANDARD™ Q CHIKUNGUNYA IGM/IGG TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 1ef8ec7d8a8b7c34dd02408bd7ebfa04 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
1ef8ec7d8a8b7c34dd02408bd7ebfa04
STANDARD™ Q CHIKUNGUNYA IGM/IGG TEST
INVIMA Analysis ID: 1ef8ec7d8a8b7c34dd02408bd7ebfa04
Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
1ef8ec7d8a8b7c34dd02408bd7ebfa04
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.SName (English)
QUIMIOLAB S.A.S

