BEUDAMED
    8 results · 27ms · 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

    P.F.C. POROUS FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code JWH·October 22, 1996

    VITROS 350 CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·June 10, 2014

    ENDOTAK C

    FDA Adverse Event
    Injury ·HISTORICAL CPI ST. PAUL·Product code NVY·October 11, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 10, 2012