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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Quadra Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Quadra Assura MP Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Unify Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Unify Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Unify Quadra Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Merlin PCS programmer Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Merlin PCS Programmer Software Cardiovascular Devices St Jude Medical Inc. 2 United States USFDA
Merlin PCS Programmer Software Cardiovascular Devices St Jude Medical Inc. 2 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 HeartMate II Left Ventricular Assist System Cardiovascular Devices Thoratec Corporation 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 SUPERA VERITAS Gastroenterology-Urology Devices IDEV Technologies, Inc. 2 United States USFDA
Device Recall Eon Mini Charging System Neurological Devices St. Jude Medical 3 United States USFDA
Device Recall HeartMate II Implant Kit with Pocket Controller; Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall HeartMate II System Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall HeartMate II LVAD Pump and Pock Controller Kit; Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall Heart Mate II Pocket Controllers removed from packaging Cardiovascular Devices Thoratec Corporation 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