BEUDAMED
    3 results · 29ms · 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 ×

    BARDEX LUBRI-SIL ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code EZL·May 23, 2014

    RADIOLUCENT RIGHT ANGLE DRIVE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·October 29, 2012

    SCULPTRA

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·September 30, 2010