ADVIA 1800 SYSTEM. - COFEPRIS Registration 1015E2019 SSA
Access comprehensive regulatory information for ADVIA 1800 SYSTEM. (ADVIA 1800 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 1015E2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.. The device was registered on May 15, 2019.
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.
ANALIZADOR BIOQUÍMICO CLÍNICO AUTOMÁTICO QUE PUEDE REALIZAR ANÁLISIS DE SUERO, PLASMA Y ORINA HUMANOS EN MODOS DE ACCESO ALEATORIO, POR LOTES Y URGENTE, CON UNA CAPACIDAD DE 1200 ANÁLISIS FOTOMÉTRICOS POR HORA Y 600 ANÁLISIS DE ELECTROLITOS POR HORA. UTIL
AUTOMATIC CLINICAL BIOCHEMICAL ANALYZER THAT CAN PERFORM HUMAN SERUM, PLASMA AND URINE ANALYSIS IN RANDOM, BATCH AND URGENT ACCESS MODES, WITH A CAPACITY OF 1200 PHOTOMETRIC ANALYSES PER HOUR AND 600 ELECTROLYTE ANALYSES PER HOUR. USEFUL