ATELLICA TM IM CALIBRATOR C (CAL C) - COFEPRIS Registration 1504R2018 SSA
Access comprehensive regulatory information for ATELLICA TM IM CALIBRATOR C (CAL C) (ATELLICA TM IM CALIBRATOR C (CAL C)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1504R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.. The device was registered on June 13, 2018.
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.
EL ATELLICA™ IM CALIBRATOR C (CAL C) ESTÁ PREVISTO PARA USO DIAGNÓSTICO IN VITRO PARA LA CALIBRACIÓN DE LOS ENSAYOS ATELLICA™ IM VB12 Y ATELLICA™ IM FER. AGENTE DE DIAGNÓSTICO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES.
THE ATELLICA IM CALIBRATOR C (CAL C) IS INTENDED FOR IN VITRO DIAGNOSTIC USE FOR THE CALIBRATION OF THE ATELLICA IM VB12 AND ATELLICA™™™ IM FER ASSAYS. DIAGNOSTIC AGENT. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.