SISTEMA ATELLICA COAG 360
Mexico·Clase I·I. MEDICAL EQUIPMENT·SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.·Registered August 06, 2018EL SISTEMA ATELLICA COAG 360 ES UN SISTEMA TOTALMENTE AUTOMATIZADO DE COAGULACIÓN SANGUÍNEA PARA SU USO EN DIAGNÓSTICO IN VITRO. EL SISTEMA UTILIZA PLASMA HUMANO Y DISTINTAS TECNOLOGÍAS O MÉTODOS DE EVALUACIÓN CON EL FIN DE OBTENER RESULTADOS PARA EL LABO
THE ATELLICA COAG 360 SYSTEM IS A FULLY AUTOMATED BLOOD COAGULATION SYSTEM FOR USE IN IN VITRO DIAGNOSTICS. THE SYSTEM USES HUMAN PLASMA AND DIFFERENT TECHNOLOGIES OR EVALUATION METHODS IN ORDER TO OBTAIN RESULTS FOR THE LABO
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- ANALIZADOR DE COAGULACIÓN PARA DIAGNÓSTICO IN VITRO
- Trade Name (English)
- COAGULATION ANALYZER FOR IN VITRO DIAGNOSTICS
- Analysis ID
- 1890E2018 SSA
- Registration Date
- August 06, 2018
- 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 ATELLICA COAG 360 (ATELLICA COAG 360 SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1890E2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.. The device was registered on August 06, 2018.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.