BEUDAMED
    4 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 ×

    ORTHO ELISA BAR CODE READER II

    FDA Adverse Event
    Malfunction ·INTERMEC CORP.·Product code JTC·September 22, 1999

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 30, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 16, 2010

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·January 9, 2013