PENUMBRA SYSTEM® 3DREVASCULARIZATION DEVICE - COFEPRIS Registration 168C2021 SSA
Access comprehensive regulatory information for PENUMBRA SYSTEM® 3DREVASCULARIZATION DEVICE (PENUMBRA SYSTEM® 3DREVASCULARIZATION DEVICE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 168C2021 SSA and manufactured by MEDSTENT, S.A. DE C.V.. The device was registered on February 08, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
ELDISPOSITIVODEREVASCULARIZACIÓN3DESTÁDISEÑADO PARAAYUDAR ALCATÉTERDEREPERFUSIÓNAEXTRAERELTROMBOSIES NECESARIO. EL DISPOSITIVO DEREVASCULARIZACIÓN 3D SE DESPLIEGADENTRODELTROMBOYACONTINUACIÓNLORETIRAHACIAELINTERIORDELCATÉTERDEREPERFUSIÓN.
THE 3D REVASCULARIZATION DEVICE IS DESIGNED TO HELP REPERFUSION CATHETER REMOVE THE NECESSARY THROMBOSIS. THE 3D REVASCULARIZATION DEVICE IS DEPLOYED INSIDE THE THROMBUS AND THEN LORETIRAHACIATHE INSIDE OF THE REPERFUSION CATHETER.