BEUDAMED
    2,978 results · 44ms · Sources: EU EUDAMED, US FDA
    Filters FDA Registration Number: 9614453 ×

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

    FDA Pre-Market Approval
    FDA Class 3 ·Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D, Cobalt

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-l ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Eve

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

    FDA Pre-Market Approval
    FDA Class 3 ·QUICKSITE XL MODEL 1058T LEFT VENTRICULAR PACING LEAD

    PELLETHANE 75D

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OPUS PACEMAKERS (MODELS 4001, 4003, 4004, 4023, 4024)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    TECOTHANE 75D POLYURETHANE RESIN FOR PULSE GENERATOR CONNECTOR MODULES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ALTERNATE STERLIZATION PROCESS & MODIFIED DF-1 LEAD CONNECTOR (MODIFICATION)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    NANOS, PIKOS 01/E01, 01-A, E01-B, LP 01/LP E01

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MINIX 834M & MINIX ST 8331M PULSE GENERATORS (MODIFICATION)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OPUS S MODEL 4121 AND 4124 PACEMAKERS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·ENTOVIS DR, ENTOVIS DR-T, ENTOVIS SR, ENTOVIS SR-T, EVIA DR, EVIA DR-T, EVIA SR,EVIA SR-T, ESTELLA DR, ESTELLA DR-T, EST

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA classification
    FDA Class 3 ·Implantable Cardioverter Defibrillator (Non-Crt)

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 3038 FUNCTION PACT FOR ASP-II 3003 PROGRAMME

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

    FDA Pre-Market Approval
    FDA Class 3 ·SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 283 PULSE GENERATOR MODEL 370 PROGRAMMER

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

    FDA Pre-Market Approval
    FDA Class 3 ·SENSOLOG/DIALOG/ REGENCY FAMILY OF PACEMAKERS

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRITY AFX DR MODEL 5346 DUAL CHAMBER PULSE