COMBISCREEN® 11SYS PLUS - INVIMA Registration a202dd92dbba5049db5e67c2ab9075d5
Access comprehensive regulatory information for COMBISCREEN® 11SYS PLUS (COMBISCREEN® 11SYS PLUS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID a202dd92dbba5049db5e67c2ab9075d5 and manufactured by LUMIRA S.A.S. The device was registered on May 31, 2033.
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.
DETERMINACIÓN DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.
DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM.

