LIAISON® XS - COFEPRIS Registration 708E2020 SSA
Access comprehensive regulatory information for LIAISON® XS (LIAISON® XS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 708E2020 SSA and manufactured by DIASORIN MÉXICO, S.A. DE C.V.. The device was registered on June 16, 2020.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
SISTEMA DE DIAGNÓSTICO QUE MIDE LAQUIMIOLUMINISCENCIA.ESTÁDESTINADOAUNUSOEXCLUSIVAMENTEPROFESIONALPARAELDIAGNÓSTICO IN VITRO. DEBE UTILIZARSEÚNICAMENTE CON INMUNOENSAYOS PORQUIMIOLUMINISCENCIA APROBADOS PORDIASORIN S.P.A. PARA EL INSTRUMENTOLIAISON® XS.
DIAGNOSTIC SYSTEM THAT MEASURES LACHEMILUMINESCENCE. IT IS INTENDED EXCLUSIVELY FOR PROFESSIONAL USE FOR IN VITRO DIAGNOSTICS. IT SHOULD ONLY BE USED WITH PORCHEMILUMINESCENCE IMMUNOASSAYS APPROVED BY DIASORIN S.P.A. FOR THE LIAISON® XS INSTRUMENT.