BEUDAMED
    8 results · 23ms · 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 ×

    9616240-2006-00344

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

    9616240-2006-00342

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

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00346

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

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·March 19, 2013