BEUDAMED
    5 results · 20ms · 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 ×

    BIOSOFT DUO DOUBLE LOOP URETERAL STENT KIT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·September 26, 2024

    BIOSOFT DUO DOUBLE LOOP URETERAL STENT KIT

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FAD·September 26, 2024

    UNICEL DXC 800 PRO SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·May 20, 2014

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2015