BEUDAMED
    8 results · 44ms · Sources: EU EUDAMED, US FDA

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    BRAVO MULTI MODALITY SYSTEM

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

    NICOLET SUBDERMAL NEEDLE

    FDA Adverse Event
    Malfunction ·NICOLET BIOMEDICAL, INC.·Product code GXE·June 28, 1996

    VIKING II

    FDA Adverse Event
    Injury ·NICOLET BIOMEDICAL, INC.·Product code GWJ·March 10, 1995

    (NICOLET) EEG VOYAGEUR

    FDA Adverse Event
    NICOLET BIOMEDICAL INC.·Product code GWQ·February 18, 2000

    NICOLET

    FDA Adverse Event
    Malfunction ·NICOLET BIOMEDICAL INC·Product code JXE·May 29, 1998

    NICOLET

    FDA Adverse Event
    Malfunction ·NICOLET BIOMEDICAL, INC.·Product code IKN·July 26, 1999

    BMSI "MicroJack" PN 672-510000 patient interface electrode connection device used during electroencephalography (EEG) /Epilepsy Monitoring evaluations with various EEG monitoring systems. The MicroJack is used with BMSI Models 2000, 3000, 4000, 5000 & 6000, and is used with the BMSI kit upgraded with NicoletOne. Nicolet Biomedical, Inc.

    FDA Recall
    Terminated ·Nicolet Biomedical Div of Viasys Healthcare·Product code GWQ·July 17, 2007

    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