BEUDAMED
    106 results · 40ms · Sources: EU EUDAMED, US FDA

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    CAMINO NEURO CARE, INC.

    FDA Adverse Event
    Malfunction ·CAMINO LABORATORIES·Product code GWM·June 30, 1997

    CUNINO NEURO CARE INC

    FDA Adverse Event
    Malfunction ·CUNINO NEURO CARE INC·Product code GWM·January 9, 1998

    VENTRIX NL950-V

    FDA Adverse Event
    Death ·INTEGRA NEUROCARE L.L.C.·Product code HCA·March 17, 2000

    BRAVO MULTI MODALITY SYSTEM

    FDA Adverse Event
    Malfunction ·NICOLET BIOMEDICAL INC.·Product code GWQ·July 24, 2003

    Viasys Healthcare NicoletOne ICU Monitor, Modular Neurodiagnostic System (containing Axiomtek Panel PC computer system), released and installed between December 2004 and March 2007 (Axiomtek Panel PC Model Number: 2147-671) VIASYS NeuroCare Part Numbers: 842-673800, 842-673900, 982A0421 and 982A0422. Manufactured, designed, developed and marketed by VIASYS NeuroCare Inc., Madison, WI 53711

    FDA Recall
    Terminated ·Nicolet Biomedical Div of Viasys Healthcare·Product code GWQ·September 11, 2007

    NicoletOne vEEG System, VIASYS Healthcare, Inc., Madison, Wisconsin 53711.

    FDA Recall
    Terminated ·CareFusion·Product code GWQ·March 8, 2010

    CAMINO NEURO CARE COMPLETE ICP MONITOR KIT

    FDA Adverse Event
    Injury ·NEUROCARE GROUP CAMINO NEURO CARE INC. HEYER-SCHULTE NEUROCARE, L.P.·Product code JXG·July 1, 1997

    MICROJACK FOR BMSI/NICOLETONE LTM

    FDA Adverse Event
    Malfunction ·VIASYS NEUROCARE INC.·Product code GWQ·June 29, 2007

    CAMINO

    FDA Adverse Event
    Injury ·CAMINO NEUROCARE, INC·Product code HCA·October 29, 1996

    CAMINO

    FDA Adverse Event
    Injury ·CAMINO NEUROCARE, INC.·Product code HCA·October 29, 1996

    VENTRIX

    FDA Adverse Event
    Death ·NEURO CARE, INC.·Product code GWM·October 29, 1996

    MICRO VENTRICULAR BOLT

    FDA Adverse Event
    Injury ·CAMINO NEUROCARE, INC.·Product code GWM·February 14, 1997

    CPT BOLT

    FDA Adverse Event
    Injury ·NEURO CARE, INC.·Product code GWM·December 18, 1998

    PUDENZ PERITONEAL LOW PRESSURE CATHETER

    FDA Adverse Event
    Malfunction ·HEYER-SCHULTE NEUROCARE INC.·Product code GBW·March 28, 2002

    LUMBAR CATHETER CLOSED TIP 80CM

    FDA Adverse Event
    Malfunction ·HEYER-SCHULTE NEUROCARE INC.·Product code JXG·March 28, 2002

    HERMETIC LARGE STYLE VENTRICULAR CATHETER SET

    FDA Adverse Event
    Malfunction ·HEYER SCHULTE NEUROCARE INC·Product code JXG·February 7, 2002

    TRAUMACATH, EXTERNAL VENTRICULAR DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·HEYER SCHULTE NEUROCARE INC·Product code JXG·February 6, 2002

    SUNDT EXTERNAL CAROTID SHUNT

    FDA Adverse Event
    Malfunction ·HEYER-SCHULTE NEUROCARE, INC.·Product code DWF·February 25, 2002

    PUDENZ VALVE

    FDA Adverse Event
    Malfunction ·HEYER SCHULTE NEUROCARE INC·Product code JXG·January 16, 2003

    PUDENZ VENTRICULAR CATHETER

    FDA Adverse Event
    Injury ·HEYER-SCHULTE NEUROCARE, INC·Product code HCA·June 22, 1999