BEUDAMED
    9 results · 48ms · 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.
    Filters Status: Injury ×

    MORTARA INSTRUMENTS, INC. / QUINTON/QTEL TELEMETRY

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code DSI·June 6, 2017

    SURVEYOR CENTRAL

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code MHX·March 17, 2016

    SURVEYOR CENTRAL

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code MHX·March 22, 2016

    SURVEYOR CENTRAL

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC·Product code MHX·February 25, 2016

    MORTARA

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC·Product code DPS·September 20, 2018

    MORTARA SOFTWARE

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code DRX·September 18, 2018

    TMX425

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code IOL·May 11, 2018

    SURVEYOR CENTRAL

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code MHX·October 2, 2015

    SURVEYOR CENTRAL

    FDA Adverse Event
    Injury ·MORTARA INSTRUMENT, INC.·Product code MHX·October 2, 2015