BEUDAMED
    20 results · 49ms · Sources: EU EUDAMED, US FDA

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    INSTRUMENT MAKAR INC

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code HWB·June 25, 1999

    HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·July 21, 2000

    HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·May 19, 2000

    INSTRUMENT MAKAR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEN·May 26, 1999

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·September 18, 1997

    THE COAGULATOR

    FDA Adverse Event
    INSTRUMENT MAKAR, INC.·Product code HQO·April 2, 1993

    BLACK PROBE

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code HRX·November 21, 1996

    HOOK TIP TIP ONLY COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·November 18, 1996

    MEDIUM STAPLE

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC·Product code GAG·February 10, 1997

    HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·February 10, 1997

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    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·January 2, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·March 13, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·February 27, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·February 13, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·February 23, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·June 5, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·April 17, 1998

    HAND-HELD HOOK TIP COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTRUMENT MAKAR, INC.·Product code GEI·April 3, 1998

    HOOK TIP HAND CONTROLLED COAGULATOR

    FDA Adverse Event
    Malfunction ·INSTUMENT MAKAR, INC.·Product code GEI·September 16, 1996

    MDSS GmbH

    Authorized representative
    🇩🇪 Germany·388 Manufacturers·16562 Devices