LIAISON TESTOSTERONA - COFEPRIS Registration 2066R2018 SSA
Access comprehensive regulatory information for LIAISON TESTOSTERONA (TESTOSTERONE LIAISON) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2066R2018 SSA and manufactured by DIASORIN MÉXICO, S.A. DE C.V.. The device was registered on August 23, 2018.
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 ENSAYO LIAISON TESTOSTERONA ES UN UNMUNOENSAYO COMPETITIVO DIRECTO POR QUIMIOLUMINISCENCIA CUYA FINALIDAD ES LA DETERMINACIÓN CUANTITATIVA DE TESTOSTERONA EN SUERO Y PLASMA HUMANS. AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIO CLÍ
THE TESTOSTERONE LIAISON ASSAY IS A DIRECT COMPETITIVE CHEMILUMINESCENCE ASSAY WHOSE PURPOSE IS THE QUANTITATIVE DETERMINATION OF TESTOSTERONE IN HUMAN SERUM AND PLASMA. IN VITRO DIAGNOSTIC AGENT. FOR EXCLUSIVE USE OF LABORATORIO CLÍ