MPA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered October 12, 2020PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DEL ÁCIDO MICOFENÓLICOTOTALENSUEROOPLASMAENLOSSISTEMASROCHE
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF MYCOPHENOLIC ACID TOTALENSERUM OPLASMA IN ROCHE SYSTEMS
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA LA DETERMINACIÓNDE ÁCIDO MICOFENÓLICO
- Trade Name (English)
- TEST FOR THE DETERMINATION OF MYCOPHENOLIC ACID
- Analysis ID
- 1385R2020 SSA
- Registration Date
- October 12, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
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.