STANDARD™ Q COVID/FLU AG COMBO TEST - INVIMA Registration 7c3b79b1dd7af000197adc0d24f7062b

Access comprehensive regulatory information for STANDARD™ Q COVID/FLU AG COMBO TEST (STANDARD™ Q COVID/FLU AG COMBO TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 7c3b79b1dd7af000197adc0d24f7062b 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.