BEUDAMED
    10,000 results · 63ms · 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 Regulation: Us FDA ×

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·May 26, 2021

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·May 31, 2021

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·May 25, 2021

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·October 6, 2021

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·April 15, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·June 30, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·June 22, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·May 19, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·April 6, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·June 8, 2022

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·October 28, 2021

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·May 31, 2022

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code GKN·September 17, 2015

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·July 12, 2024

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·July 22, 2024

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·July 17, 2024

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·August 8, 2024

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·September 30, 2024

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code GKN·October 27, 2020

    ACT PLUS INSTRUMENT

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code GKN·June 30, 2022