BEUDAMED
    96 results · 30ms · Sources: EU EUDAMED, US FDA

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    PHACO CHOP NEEDLES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    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·April 21, 1999

    IMPORT WITH USER-ATTACHABLE 9.5F BIOGLIDE CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC PS MEDICAL·Product code LJT·March 5, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 21, 1999

    RESTORE 4X13 TPS CYLINDER IMPLANT

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

    RESTORE 4X15 TPS SCREW IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 11, 1998

    SOFTFORM FACIAL IMPLANT

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

    RESTORE 4X13 TPS SCREW IMPLANT

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

    NEEDLE 27GA X 103MM WHITACRE BULK

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code FMI·May 18, 2021

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·July 9, 1999

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·October 29, 1997

    CATHETER

    FDA Adverse Event
    Other ·MEDTRONIC, INC.·Product code LKK·January 31, 1997

    RESTORE 4X15 SELF-TAPPING IMPLANT WITH MOUNT

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

    SOFTFORM FACIAL IMPLANT

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

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·October 17, 1997

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·October 29, 1997

    ENDOPATH DILATING TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. S.A DE C.V.·Product code GCJ·November 13, 1998

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·October 31, 1997