1. STANDARD™ ADENO RESPI AG TEST - INVIMA Registration ea55a7d8f8c57db7dedd6a248ce269ae

Access comprehensive regulatory information for 1. STANDARD™ ADENO RESPI AG TEST (1. STANDARD™ ADENO RESPI AG TEST) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID ea55a7d8f8c57db7dedd6a248ce269ae and manufactured by QUIMIOLAB S.A.S. The device was registered on June 12, 2034.

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.