BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PORTEX TRACHEAL TUBE CLEAR MURPHEY EYESOFT SEAL

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code BTR·July 18, 2025

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    CSF - CARDIAC/PERITONEAL CATHETER, STD. BARIUM IMPR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·April 11, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 15, 2011

    CELL-DYN 1700

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELL DYN·Product code GKZ·June 12, 2008

    NON-VENTED HOSPITAL FULL FACE MASK

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code MNT·April 26, 2017