LIAISON® AFP - COFEPRIS Registration 2208R2019 SSA

Access comprehensive regulatory information for LIAISON® AFP (LIAISON® AFP) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2208R2019 SSA and manufactured by DIASORIN MÉXICO S.A. DE C.V.. The device was registered on December 04, 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.