BEUDAMED
    6 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 ×

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·February 15, 2011

    HEARTMATE IMPLANTABLE PNEUMATIC LEFT VENTRICULAR ASSIST SYST

    FDA Adverse Event
    Injury ·THERMO CARDIOSYSTEMS, INC.·Product code DSQ·June 19, 1998

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·February 13, 2013

    MP70

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 21, 2010

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 28, 2014

    ZENITH TX2 DISSECTION ENDOVASCULAR GRAFT STRAIGHT COMPONENT

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code MIH·November 11, 2024