BEUDAMED
    3 results · 27ms · 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 ×

    HIWIRE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DQX·May 29, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012

    PUMP MMT-722RNAP PRDGM INS PL EN RC

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 29, 2010