MPA - COFEPRIS Registration 1385R2020 SSA
Access comprehensive regulatory information for MPA (MPA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1385R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on October 12, 2020.
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.
PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DEL ÁCIDO MICOFENÓLICOTOTALENSUEROOPLASMAENLOSSISTEMASROCHE
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF MYCOPHENOLIC ACID TOTALENSERUM OPLASMA IN ROCHE SYSTEMS