BEUDAMED
    3 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 ×

    EXPRESSEW FLEXIBLE SUTURE PASSER NEEDLE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HRX·October 4, 2010

    5.5MM HEX-END ROD 500MM

    FDA Adverse Event
    Death ·SYNTHES GMBH·Product code NKB·December 20, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 30, 2014