PRUEBA PARA LA DETECCIÓN DE LA PROTEÍNA QUINASA DEL LINFOMA ANAPLÁSICO (ALK). - COFEPRIS Registration 1417R2024 SSA

Access comprehensive regulatory information for PRUEBA PARA LA DETECCIÓN DE LA PROTEÍNA QUINASA DEL LINFOMA ANAPLÁSICO (ALK). (PRUEBA PARA LA DETECCIÓN DE LA PROTEÍNA QUINASA DEL LINFOMA ANAPLÁSICO (ALK).) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1417R2024 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on May 16, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.