BEUDAMED
    5 results · 19ms · 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 ×

    ZIMMER

    FDA Adverse Event
    Injury ·ZIMMER·Product code KWB·December 20, 1996

    TOTAL HIP PROSTHESIS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·January 4, 1996

    CS300

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 9, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 8, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-REDWOOD CITY·Product code MGB·November 18, 2010