BEUDAMED
    10 results · 34ms · 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 ×

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code FZP·June 7, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 15, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 8, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code FZP·June 7, 2006

    CLOSED KNOT PUSHER

    FDA Adverse Event
    Malfunction ·BIOMET SPORTS MEDICINE, INC.·Product code HXO·September 9, 2010

    TI LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKG·June 23, 2017

    LIGAMAX CLIP APPLIER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 10, 2014

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 11, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·December 10, 2012

    TI LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKG·June 23, 2017