NEPHSTAR TRANSFERRIN (TRF) /NEPHSTAR TRF KIT - COFEPRIS Registration 992R2021 SSA
Access comprehensive regulatory information for NEPHSTAR TRANSFERRIN (TRF) /NEPHSTAR TRF KIT (NEPHSTAR TRANSFERRIN (TRF) /NEPHSTAR TRF KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 992R2021 SSA and manufactured by KABLACOMERCIAL,S.A.DE C.V.. The device was registered on November 06, 2021.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
ESTE PRODUCTO SE UTILIZA EN ELANALIZADOR DE PROTEÍNAS ESPECÍFICASNEPHSTAR® PARA LA DETERMINACIÓNCUANTITATIVA DE LA TRANSFERRINA (TRF)HUMANA EN SUERO COMO AYUDA EN ELDIAGNÓSTICO DE SU METABOLISMOANORMAL. AGENTE DE DIAGNÓSTICO INVITRO PARA USO EXCLUSIVO DELABORATORIOS CLÍNICOS O DE GABINETE.
THIS PRODUCT IS USED IN THE NEPHSTAR® SPECIFIC PROTEIN ANALYZER FOR THE QUANTITATIVE DETERMINATION OF HUMAN TRANSFERRIN (TRF) IN SERUM AS AN AID IN THE DIAGNOSIS OF ITS NORMAL METABOLISM. INVITRO DIAGNOSTIC AGENT FOR EXCLUSIVE USE OF CLINICAL OR CABINET LABORATORIES.