PRUEBA DE DETECCIÓN DE ARNM CITOPLÁSMICO
Mexico·Clase II·III. Agentes de
diagnóstico·PRODUCTOS ROCHE, S.A.
DE C.V.·Registered February 08, 2024- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- VENTANA INFORM CYTOPLASMIC LAMBDA MRNA PROBE
- Trade Name (English)
- VENTANA INFORM CYTOPLASMIC LAMBDA MRNA PROBE
- Analysis ID
- 0453R2024 SSA
- Registration Date
- February 08, 2024
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA DE DETECCIÓN DE ARNM CITOPLÁSMICO (PRUEBA DE DETECCIÓN DE ARNM CITOPLÁSMICO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0453R2024 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on February 08, 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.