REVERSE T3 (RT3) ELISA - INVIMA Registration fb25a091884b435b35c501f8d00a5716
Access comprehensive regulatory information for REVERSE T3 (RT3) ELISA (REVERSE T3 (RT3) ELISA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID fb25a091884b435b35c501f8d00a5716 and manufactured by BYO COLOMBIA S.A.S.. The device was registered on September 06, 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.
PARA LA MEDICIÓN CUANTITATIVA DE TRIYODOTIRONINA _x000D_ INVERSA (RT3) EN SUERO Y PLASMA HUMANOS MEDIANTE _x000D_ UN ELISA (ENSAYO INMUNOABSORBENTE LIGADO A _x000D_ ENZIMAS). ESTE KIT ESTÁ DISEÑADO SOLO PARA USO _x000D_ PROFESIONAL Y SOLO PARA USO EN LABORATORIO. PARA _x000D_ DIAGNÓSTICO IN VITRO ONLY. DISEÑADO PARA SER _x000D_ UTILIZADO MANUALMENTE, PERO PUEDE SER ADAPTABLE A_x000D_ ANALIZADORES AUTOMÁTICOS ABIERTOS. EL USUARIO ES _x000D_ RESPONSABLE DE VALIDAR EL RENDIMIENTO DE ESTE KIT _x000D_ CON CUALQUIER ANALIZADOR AUTOMATIZADO.
FOR THE QUANTITATIVE MEASUREMENT OF TRIIODOTHYRONINE _x000D_ REVERSE (RT3) IN HUMAN SERUM AND PLASMA BY _x000D_ AN ELISA (_x000D_-LINKED IMMUNOSORBENT ASSAY ENZYMES). THIS KIT IS INTENDED FOR _x000D_ USE ONLY PROFESSIONAL AND FOR LABORATORY USE ONLY. FOR _x000D_ IN VITRO DIAGNOSTICS ONLY. DESIGNED TO BE _x000D_ USED MANUALLY, BUT CAN BE ADAPTABLE A_x000D_ OPEN AUTOMATIC ANALYZERS. THE USER IS _x000D_ RESPONSIBLE FOR VALIDATING THE PERFORMANCE OF THIS KIT _x000D_ WITH ANY AUTOMATED ANALYZER.