BEUDAMED
    94 results · 32ms · Sources: EU EUDAMED, US FDA

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    ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SOFTFORM FACIAL IMPLANT

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

    METRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

    HORIZONS CYTOLOGY BRUSH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    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·April 21, 1999

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·STRATO/INFUSAID, INC.·Product code LJT·August 5, 1998

    RESTORE 3.3X15 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 21, 1998

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 10, 1998

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·October 2, 1998

    SOFTFORM FACIAL IMPLANT

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

    PONSKY NON-BALLOON G-TUBE

    FDA Adverse Event
    Malfunction ·BIPD DIV., CR BARD·Product code KNT·July 23, 1999

    SOFTFORM FACIAL IMPLANT

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

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·STRATO/INFUSAID, INC.·Product code LJT·August 5, 1998

    INTERLINK CONTINU-FLO SOLUTION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FPA·August 26, 1998

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·October 30, 1998

    CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code LWR·May 6, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·August 11, 1998

    INDIGO 1 CM FIBER

    FDA Adverse Event
    Death ·INDIGO MEDICAL, INC.·Product code GEX·August 19, 1998

    RESTORE 3.75X13 TPS SCREW IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·November 19, 1998