BEUDAMED
    7 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 ×

    GLUCOSE MONITORING SYS/KIT

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 18, 2014

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·September 20, 2012

    SIMPLEX P - US TOBRA FD 10-PK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·July 12, 2010

    COMP PRIMARY STEM 14MM MINI

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·June 10, 2020

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 7, 2020

    CR VIVACIT-E 36MM BRNG STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 7, 2020

    MINI TRAY STD COCR +3 OFFSET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 7, 2020