STRYKER CORE 2
Mexico·Clase II·I. MEDICAL EQUIPMENT·STRYKER MÉXICO, S.A. DE C.V.·Registered March 28, 2018LA 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
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- CONSOLA
- Trade Name (English)
- CONSOLE
- Analysis ID
- 838E2018 SSA
- Registration Date
- March 28, 2018
- Name (Spanish)
- STRYKER MÉXICO, S.A. DE C.V.
- Name (English)
- STRYKER MEXICO, S.A. DE C.V.
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.