SISTEMA ACELERADOR LINEAL
Mexico·Clase III·I. Equipo Médico·SIEMENS HEALTHCARE
DIAGNOSTICS, S. DE R.L. DE
C.V.·Registered March 26, 2024- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- I. Equipo Médico
- Product Type (English)
- I. Equipo Médico
- Trade Name (Spanish)
- HIGH ENERGY TREATMENT (PLATAFORMA HET)
- Trade Name (English)
- HIGH ENERGY TREATMENT (PLATAFORMA HET)
- Analysis ID
- 0878E2024 SSA
- Registration Date
- March 26, 2024
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
Access comprehensive regulatory information for SISTEMA ACELERADOR LINEAL (SISTEMA ACELERADOR LINEAL) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0878E2024 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on March 26, 2024.
This page provides complete registration details including product type (I. Equipo Médico), 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.