TARGET - COFEPRIS Registration 862C2019 SSA
Access comprehensive regulatory information for TARGET (TARGET) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 862C2019 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on April 25, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.
LAS ESPIRALES DESMONTABLES TARGET ESTÁN PENSADAS PARA OBSTRUIR O TAPONAR ENDOVASCULARMENTE EL FLUJO SANGUÍNEO EN ANOMALÍAS VASCULARES DE LOS VASOS NEUROVASCULARES Y PERIFÉRICOS. LAS ESPIRALES DESMONTABLES TARGET ESTÁN INDICADAS PARA LA EMBOLIZACIÓN ENDOVA
TARGET REMOVABLE COILS ARE INTENDED TO OBSTRUCT OR ENDOVASCULARLY PLUG BLOOD FLOW IN VASCULAR ABNORMALITIES OF NEUROVASCULAR AND PERIPHERAL VESSELS. TARGET REMOVABLE COILS ARE INDICATED FOR ENDOVA EMBOLIZATION