BEUDAMED
    3 results · 20ms · 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 ×

    UNKNOWN M2A HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 16, 2014

    CORAIL2 STD SIZE 11

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 17, 2012

    VITAL-PORT DETACHED SILICONE CATHETER TITANIUM INFUSION PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC.·Product code DWF·June 25, 2015