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STANDARD™Q INFLUENZA A/B TEST - INVIMA Registration 7453b36d750b9ca9b282bb8b737f0597

Access comprehensive regulatory information for STANDARD™Q INFLUENZA A/B TEST (STANDARD™Q INFLUENZA A/B TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 7453b36d750b9ca9b282bb8b737f0597 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
7453b36d750b9ca9b282bb8b737f0597
STANDARD™Q INFLUENZA A/B TEST
INVIMA Analysis ID: 7453b36d750b9ca9b282bb8b737f0597
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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
7453b36d750b9ca9b282bb8b737f0597
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S