BEUDAMED
    4 results · 18ms · 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 ×

    MENTOR MEMORYSHAPE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 23, 2019

    VA LOCKSCR Ø2.4 SELF-TAP L20 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HRS·January 22, 2013

    ENPULSE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·December 14, 2010

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 9, 2014