Vista de la lista Vista de las tarjetas
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Proclaim Elite SCS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG with MDT header Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG with MDT header Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Proclaim DRG Implantable Pulse Generator Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Eon Mini" Implantable Pulse Generator (IPG) Neurological Devices Advanced Neuromodulation Systems, Inc 3 United States USFDA
Device Recall Eon Mini Neurostimulation (IPG) System Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Device Recall Eon Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Device Recall Eon Mini Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Device Recall Brio DBS System Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Device Recall Eon Mini Neurological Devices St. Jude Medical 3 United States USFDA
Device Recall Eon Charging System Neurological Devices St. Jude Medical 3 United States USFDA
Device Recall Eon and Eon Mini Neurological Devices St. Jude Medical 3 United States USFDA
Device Recall Eon Mini Charging System Neurological Devices St. Jude Medical 3 United States USFDA
Device Recall Percutaneous Trial Lead Kits Neurological Devices St. Jude Medical, Inc. 2 United States USFDA
Device Recall Percutaneous Trial Lead Kits Neurological Devices St. Jude Medical, Inc. 2 United States USFDA
Device Recall Eon IPG Neurological Devices Advanced Neuromodulation Systems, Inc 3 United States USFDA
Device Recall SwiftLock Anchor, Model 1192 Neurological Devices Advanced Neuromodulation Systems, Inc 2 United States USFDA
Device Recall Eon Mini Neurostimulation Sysem Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Device Recall Rapid Programmer Neurological Devices Advanced Neuromodulation Systems 3 United States USFDA
Eon Mini 3788 (IPG) Neurological Devices Advanced Neuromodulation Systems Inc. 3 United States USFDA
Neuromodulation systems Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Neuromodulation systems Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Neuromodulation systems Neurological Devices St. Jude Medical, Inc. 3 United States USFDA