BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNK_QDOT MICRO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 10, 2022

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·March 19, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·January 18, 2011

    RIATA PASSIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    BLUNT TIP SCREW, 4X38MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·June 8, 2021

    REVERSE SHOULDER SYSTEM GLENOID BASEPLATE Ø27X25

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·June 19, 2024