BEUDAMED
    3 results · 20ms · 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 ×

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 9, 2014

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Death ·DEPUY INTERNATIONAL·Product code KWA·November 6, 2012

    CE INTERMATE LV 100, 24 PACK,50126

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·August 30, 2010