BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 30, 2013

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 11, 2017

    METER C - OT PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·February 7, 2002

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·July 5, 2000

    LASER FLEX

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL·Product code BTR·August 25, 1998

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code GEI·December 16, 2025

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code GEI·December 16, 2025

    PROLENE SUT 24IN(60CM) 6-0 BLU

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·August 5, 2019

    PROLENE SUT 24IN(60CM) 6-0 BLU

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·August 5, 2019

    PROLENE SUT 24IN(60CM) 6-0 BLU

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·August 5, 2019

    PROLENE SUT 24IN(60CM) 6-0 BLU

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·August 5, 2019

    STENTS I-CAST

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code JCT·October 9, 2023