BEUDAMED
    3 results · 28ms · 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 ×

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 20, 2013

    UNKNOWN DEPUY ASR XL ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·DEPUY IINTL, LTD.·Product code KWA·January 20, 2011