BEUDAMED
    1,962 results · 45ms · Sources: EU EUDAMED, US FDA

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    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 23, 2020

    NUROLON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·October 31, 2018

    BICAP, HEMOSTASIS PROBE

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code FEH·June 7, 2021

    ENDOPATH ELECTROSURGERY PROBE PLUS II

    FDA Adverse Event
    Other ·ETHICON ENDOSURGERY·Product code FEH·March 29, 1994

    ELECTROSURGICAL GENERATOR (E.S.U.)

    FDA Adverse Event
    Malfunction ·VALLEYLAB, INC.·Product code FEH·January 9, 1994

    UNIVERSAL TRUMPET VALVE

    FDA Adverse Event
    Injury ·CARDINAL HEALTH, CANADA, INC.·Product code FEH·July 9, 2004

    CATHETER, IRRIGATION

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FEH·December 21, 2017

    ENDOCOAGULATOR

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FEH·January 25, 1995

    SEMM POINT COAGULATOR

    FDA Adverse Event
    Malfunction ·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FEH·January 26, 1995

    BICAP HEMOSTASIS PROBE 7FR

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code FEH·July 20, 2020

    VALLEYLAB

    FDA Adverse Event
    Injury ·VALLEYLAB, INC.·Product code FEH·September 5, 1997

    ENDOPATH ELECTRO SURGERY PROBE PLUS II

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FEH·July 8, 1997

    CONMED

    FDA Adverse Event
    Injury ·CONMED ELECTROSURGERY·Product code FEH·August 30, 2007

    CONMED

    FDA Adverse Event
    Injury ·CONMED ELECTROSURGERY·Product code FEH·August 15, 2007

    TRUMPET VALVE

    FDA Adverse Event
    Other ·DAVIS & GECK·Product code FEH·April 14, 1994

    CMC II COAGULATOR (80-1140)

    FDA Adverse Event
    CODMAN & SHURTLEFF INC.·Product code FEH·August 20, 1992

    A&E MEDICAL CORPORATION - SUCTION COAGULATOR

    FDA Adverse Event
    Injury ·A&E MEDICAL CORPORATION·Product code FEH·August 10, 2017

    7FR 300CM BIPOLAR HEMO PROBE

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code FEH·April 12, 2018

    VALLEYLAB

    FDA Adverse Event
    Injury ·COVIDIEN / VALLEYLAB·Product code FEH·December 16, 2013

    Electrode, Flexible Suction Coagulator

    FDA classification
    FDA Class 2 ·Electrode, Flexible Suction Coagulator