STRYKER SISTEMA F1 - COFEPRIS Registration 251E2019 SSA
Access comprehensive regulatory information for STRYKER SISTEMA F1 (STRYKER F1 SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 251E2019 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on February 12, 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.
EL SISTEMA F1 DE STRYKER (F1 SYSTEM) ESTÁ INDICADO PARA TALADRAR Y CORTAR TEJIDO ÓSEO Y DURO, ASÍ COMO PARA COLOCAR ALAMBRES Y TORNILLOS DE DICHOS TEJIDOS. EL SISTEMA ESTÁ DISEÑADO PARA APLICACIONES QUIRÚRGICAS ORTOPÉDICAS DE TRAUMATOLOGÍA, CIRUGÍA DE M
STRYKER'S F1 SYSTEM IS INDICATED FOR DRILLING AND CUTTING BONE AND HARD TISSUE, AS WELL AS FOR LAYING WIRES AND SCREWS FROM SUCH TISSUES. THE SYSTEM IS DESIGNED FOR ORTHOPEDIC SURGICAL APPLICATIONS OF TRAUMATOLOGY, SURGERY OF