STANDARD™ Q COVID-19 AG TEST 2.0 - INVIMA Registration f73b7e9f4918ac659a68df315790f88a

Access comprehensive regulatory information for STANDARD™ Q COVID-19 AG TEST 2.0 ( STANDARD™ Q COVID-19 AG TEST 2.0) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID f73b7e9f4918ac659a68df315790f88a 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.