BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DWF·November 1, 2017

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·August 5, 2013

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·August 5, 2013

    BRONCHO-CATH ENDOBRONCHIAL TUBE, LEFT SIDED 39FR.

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code CBI·September 4, 1997

    LARYNGEAL MASK AIRWAY

    FDA Adverse Event
    Malfunction ·THE LARYNGEAL MASK COMPANY·Product code CAE·February 27, 2001

    VENOUS BLOODLINE NON-MACHINE SPECIFIC

    FDA Adverse Event
    Malfunction ·ERIKA DE REYNOSA·Product code FJK·March 25, 1999

    TD TORQUE LINE CATHETER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code DYG·January 10, 2013

    HEARTMATE II LVAS

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·November 21, 2016

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 14, 2026