URINALYSIS CONTROLS CHEK-STIX LIQUID QC KIT - INVIMA Registration ee77e0fe0b895f9734717d904f051855
Access comprehensive regulatory information for URINALYSIS CONTROLS CHEK-STIX LIQUID QC KIT (URINALYSIS CONTROLS CHEK-STIX LIQUID QC KIT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID ee77e0fe0b895f9734717d904f051855 and manufactured by SIEMENS HEALTHCARE 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.
CHEK-STIX® LIQUID QC KIT ES UN PRODUCTO LÍQUIDO _x000D_ LISTO PARA USAR DESTINADO A SER UTILIZADO EN _x000D_ ENTORNOS DE LABORATORIOS CENTRALES COMO _x000D_ CONTROL PARA PROCEDIMIENTOS CUALITATIVOS Y _x000D_ SEMICUANTITATIVOS UTILIZADOS EN DETERMINACIONES_x000D_ FISICOQUÍMICAS Y QUÍMICAS DE LA ORINA HUMANA. PARA _x000D_ USO EXCLUSIVO EN CLINITEK NOVUS®.
CHEK-STIX® LIQUID QC KIT IS A LIQUID PRODUCT _x000D_ READY-TO-USE INTENDED FOR USE IN _x000D_ CENTRAL LAB ENVIRONMENTS SUCH AS _x000D_ CONTROL FOR QUALITATIVE AND _x000D_ PROCEDURES SEMI-QUANTITATIVE USED IN DETERMINACIONES_x000D_ PHYSICOCHEMICAL AND CHEMICAL MEASUREMENTS OF HUMAN URINE. FOR _x000D_ EXCLUSIVE USE AT CLINITEK NOVUS.®