BEUDAMED
    77 results · 23ms · Sources: EU EUDAMED, US FDA

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    MODEL J-5 MVO-MONITOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 12, 1998

    POWDER-FREE LAVENDER/PURPLE NITRILE EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·July 22, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 29, 1998

    RESTORE 3.75X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·November 30, 1998

    SUSTAIN 4.2X13 MC EXTERNAL HEX HA IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 18, 1998

    CERVICAL SPINE LOCKING PLATE/26MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·September 8, 1998

    LP6+VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 31, 1998

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·July 1, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC·Product code FTL·June 18, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 25, 1998

    FASTRACKER-18

    FDA Adverse Event
    Malfunction ·TARGET THERAPEUTICS/A BOSTON SCIENTIFIC CO·Product code DQO·June 30, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·January 8, 1999

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·October 30, 1997

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998

    STOCKERT SYSTEM 3 ROLLER PUMP MODULE

    FDA Adverse Event
    Malfunction ·STOCKERT INSTRUMENTE·Product code DWB·August 24, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC·Product code FTL·November 12, 1998

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·August 22, 1997