LIAISON ANALYZER. - COFEPRIS Registration 637E2018 SSA

Access comprehensive regulatory information for LIAISON ANALYZER. (LIAISON ANALYZER.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 637E2018 SSA and manufactured by DIASORIN MÉXICO, S.A. DE C.V.. The device was registered on March 02, 2018.

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.