BEUDAMED
    9 results · 25ms · 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 Status: Malfunction ×

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    9616240-2006-00339

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00340

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00350

    FDA Adverse Event
    Malfunction ·Product code FII·June 23, 2006

    9616240-2006-00345

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 10, 2010