NEPHSTAR® K LIGHT CHAIN KIT. - COFEPRIS Registration 1559R2021 SSA
Access comprehensive regulatory information for NEPHSTAR® K LIGHT CHAIN KIT. (NEPHSTAR® K LIGHT CHAIN 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 1559R2021 SSA and manufactured by KABLACOMERCIAL,S.A.DE C.V.. The device was registered on May 10, 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.
LA PRUEBA SE UTILIZA PARA LADETERMINACIÓN CUANTITATIVA DE LACADENALIVIANAKAPPA(KAP)(INCLUIDASLACADENALIVIANALIBREYLACADENALIVIANAUNIDA)HUMANAENSUEROCOMOAYUDAENEL DIAGNÓSTICO DE SU METABOLISMOANORMAL
THE TEST IS USED FOR THE QUANTITATIVE DETERMINATION OF THE HUMAN LIGHT CHAINNAKAPPA(KAP) (INCLUDING THE FREE LIGHT CHAIN AND THE UNITED LIGHT CHAIN) IN SERUM AS AN AID IN THE DIAGNOSIS OF ITS NORMAL METABOLISM