FTD FEVER AND RASH
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered March 14, 2019ENSAYO PARA DETERMINAR ACIDOS NUCLEICOS
NUCLEIC ACID ASSAY
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA DETERMINAR ACIDOS NUCLEICOS
- Trade Name (English)
- NUCLEIC ACID ASSAY
- Analysis ID
- 542R2019 SSA
- Registration Date
- March 14, 2019
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR
Access comprehensive regulatory information for FTD FEVER AND RASH (FTD FEVER AND RASH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 542R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 14, 2019.
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.