BEUDAMED
    117 results · 26ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application

    Leadless Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Micra VR/AV Application

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Platform, CareLink SmartSync Host Application, CareLink SmartSync Common Application, CareLink SmartS

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·GUIDANT CONTAK RENEWAL FAMILY OF CARDIAC RESYNCHRONIZATION THERAPY DEVICES

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·GUIDANT VITALITY FAMILY OF IMPLANTABLE CARDIOVERTER DEFIBRILLATORS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DISCOVERY/MERIDIAN

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application

    Stimulator, Autonomic Nerve, Implanted (Depression)

    FDA Pre-Market Approval
    FDA Class 3 ·CYBERONICS VNS THERAPY SYSTEM

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·REPLY SR, REPLY DR, ESPRIT SR, ESPRIT DR

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PARADYM (VR/DR) 8750, PARADYM RF (VR/DR) 9750(ZL101),PARADYM RF (VR/DR) 9750 (ZL102),INTENSIA (VR/DR)

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·PARADYM CRT-D 8750,PARADYM RF CRT-D 9750 (ZL101), PARADYM RF CRT-D 9750 (ZL 102) AND INTENSIA CRT-D

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHAGMATIC/PHRENIC NERVE STIMULATOR

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA Pre-Market Approval
    FDA Class 3 ·DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR