BEUDAMED
    89 results · 22ms · Sources: EU EUDAMED, US FDA

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    BISCOVER LED

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRIPPER PLUS NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·August 20, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·February 3, 1999

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·April 23, 1999

    ETHICON, INC./JOHNSON & JOHNSON

    FDA Adverse Event
    Injury ·ETHICON, INC./JOHNSON & JOHNSON·Product code GAM·March 23, 2000

    HYDROVIEW INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·May 12, 2003

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    ASSURANCE 2000 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·February 5, 1999

    *

    FDA Adverse Event
    Injury ·DATASCOPE CORP. CARDIAC ASSIST·Product code DSP·January 26, 1999

    ASSURANCE 2000 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·February 5, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    DATASCOPE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. CARDIAC ASSIST·Product code DSP·January 26, 1999

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·April 22, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·November 4, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·February 3, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·November 4, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 15, 1999