STRYKER SYSTEM G - COFEPRIS Registration 1930E2018 SSA
Access comprehensive regulatory information for STRYKER SYSTEM G (STRYKER SYSTEM G) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1930E2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on August 07, 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.
STRYKER SYSTEM G ESTÁ INDICADO PARA USARSE EN PROCEDIMIENTOS QUIRÚRGICOS EN LOS QUE HAYA QUE ESCARIAR, PERFORAR, CORTAR, DESCORTEZAR O FIJAR CON TORNILLOS TEJIDO DURO O HUESO.
STRYKER SYSTEM G IS INDICATED FOR USE IN SURGICAL PROCEDURES INVOLVING REAMING, DRILLING, CUTTING, DEBARKING OR SCREWING HARD TISSUE OR BONE.