FA50 - COFEPRIS Registration 1580E2019 SSA

Access comprehensive regulatory information for FA50 (FA50) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1580E2019 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on August 09, 2019.

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.