BEUDAMED
    8 results · 50ms · Sources: EU EUDAMED, US FDA

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    HEMOCLIP

    FDA Adverse Event
    Death ·EDWARD WECK, INC.·Product code MCH·June 2, 1992

    MONOPOLAR CAUTERY FORCEPS

    FDA Adverse Event
    Other ·EDWARD WECK, INC.·Product code GEI·April 29, 1994

    WECK NEEDLE ELECTRODE

    FDA Adverse Event
    Injury ·EDWARD WECK, INC.·Product code GXZ·July 29, 1992

    WEC-PEN

    FDA Adverse Event
    Injury ·EDWARD WECK INC.·Product code GEI·November 5, 1997

    NEEDLE ELECTRODE

    FDA Adverse Event
    Injury ·EDWARD WECK, INC.·Product code GXZ·February 10, 1993

    ELECTROSURGICAL COAGULATION SUCTION TUBE W/STYLET

    FDA Adverse Event
    Injury ·EDWARD WECK, INC.·Product code EKZ·February 15, 1993

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 13, 2023

    BLADE ELECTRODE

    FDA Adverse Event
    Malfunction ·EDWARD WEEK, INC.·Product code GEI·February 10, 1996