BEUDAMED
    197 results · 39ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VERSATRAX MODEL 7000 UNIVERSAL A-V PULSE GENERATOR

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    ADAPTA D

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·March 27, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·August 9, 2016

    ENRHYTHM

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVZ·December 23, 2014

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 22, 2016

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·February 16, 2016

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·February 23, 2016

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·February 10, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2016

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 5348 SINGLE CHAMBER TEMPORARY PACEMAKER (AAI/VVI) AND MODEL 5388 DUAL CHAMBER TEMPORARY PACEMAKER

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DISPOSABLE COVER

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·5846 DISPOSABLE PATIENT CABLE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VARIOUS FAMILIES/MODELS OF PASYS, SPECTRAX, SYMBIOS, & SYNERGYST