BEUDAMED
    73 results · 24ms · Sources: EU EUDAMED, US FDA

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    DRY LASER IMAGER, DRYPRO MODEL 832

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOFTFORM FACIAL IMPLANT

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

    MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRIPPER PLUS NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    1720159-1999-00158

    FDA Adverse Event
    Malfunction ·December 28, 1999

    SOFTFORM FACIAL IMPLANT

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

    9216 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·July 22, 1999

    9950 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·January 12, 2000

    9550 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·January 12, 2000

    SOFTFORM FACIAL IMPLANT

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

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 2, 1999

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 2, 1999

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 2, 1999

    9550 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·January 4, 2000

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Other ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·February 4, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 27, 1999

    AUTO SUTURE TA PREMIUM 30-V3 DISPOSABLE LOADING UNIT

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·June 12, 1998

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT, INC.·Product code CBK·August 6, 1999

    AUTO SUTURE DPI 30 M DISPOSABLE LOADING UNIT

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·August 5, 1999

    AUTO SUTURE ENDO CLIP 5MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·January 26, 1998