STRYKER CORE 2 - COFEPRIS Registration 838E2018 SSA
Access comprehensive regulatory information for STRYKER CORE 2 (STRYKER CORE 2) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 838E2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on March 28, 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.
LA CONSOLA CORE 2 (EQUIPO DE QUIRÓFANO CONSOLIDADO; CONSOLIDATED OPERATING ROOM EQUIPMENT) DE STRYKER ESTÁ INDICADA PARA CORTAR, TALADRAR, ESCARIAR, DESCORTEZAR, DAR FORMA Y ALISAR HUESOS, CEMENTO ÓSEO Y DIENTES EN DIVERSAS INTERVENCIONES QUIRÚRGICAS, TAL
THE CORE 2 CONSOLE (CONSOLIDATED OPERATING ROOM EQUIPMENT; STRYKER'S CONSOLIDATED OPERATING ROOM EQUIPMENT) IS INDICATED FOR CUTTING, DRILLING, REAMING, DEBARKING, SHAPING AND SMOOTHING BONES, BONE CEMENT AND TEETH IN VARIOUS SURGICAL PROCEDURES, SUCH