LIAISON® 25 OH VITAMIN D TOTAL ASSAY - COFEPRIS Registration 1251R2019 SSA
Access comprehensive regulatory information for LIAISON® 25 OH VITAMIN D TOTAL ASSAY (LIAISON® 25 OH VITAMIN D TOTAL ASSAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1251R2019 SSA and manufactured by DIASORIN MÉXICO S.A. DE C.V.. The device was registered on June 28, 2019.
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.
EL LIAISON® 25 OH VITAMIN D TOTAL ASSAY UTILIZA LA TECNOLOGÍA DE INMUNOENSAYO POR QUIMIOLUMINISCENCIA (CLIA) PARA LA DETERMINACIÓN CUANTITATIVA DE LA 25-HIDROXIVITAMINA D Y DE OTROS METABOLITOS HIDROXILADOS DE VITAMINA D EN SUERO HUMANO, PLASMA EDTA O PLA
THE LIAISON® 25 OH VITAMIN D TOTAL ASSAY USES CHEMILUMINESCENCE IMMUNOASSAY (CLIA) TECHNOLOGY FOR THE QUANTITATIVE DETERMINATION OF 25-HYDROXYVITAMIN D AND OTHER HYDROXYLATED METABOLITES OF VITAMIN D IN HUMAN SERUM, PLASMA EDTA OR PLA