BEUDAMED
    12 results · 42ms · 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 FDA Adverse Event ×

    MY01 CONTINUOUS COMPARTMENTAL PRESSURE MONITOR

    FDA Adverse Event
    Injury ·MY01 INC.·Product code LXC·October 27, 2021

    EASYPUMP 2

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·February 15, 2024

    EASYPUMP 2

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·January 3, 2024

    EASYPUMP 2

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·November 17, 2023

    EASYPUMP 2

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·December 19, 2023

    EASYPUMP® II

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code MEB·October 19, 2016

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·October 18, 2023

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·August 29, 2023

    EASYPUMP

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·August 14, 2023

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·February 9, 2024

    EASYPUMP 2

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code MEB·December 7, 2023

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·October 18, 2023