BEUDAMED
    4 results · 36ms · 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 ×

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 1, 2014

    VIPER 2 X-TAB CANNULATED SCREW 6X50MM TI 2810

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code NKB·November 6, 2012

    SCULPTRA

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·August 27, 2010

    PFNA-II BLADE L75 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·June 23, 2023