BEUDAMED
    3 results · 27ms · 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 ×

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 24, 2014

    REVEAL DX

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·October 31, 2012

    OVER THE MATTRESS SENSOR PAD

    FDA Adverse Event
    Malfunction ·POSEY MEDICAL DEVICE LTD.·Product code KMI·August 13, 2010