BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 27, 2014

    D903 DIDECO AVANT 2 VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 19, 2014

    IT PADOVA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 8, 2013

    D903 DIDECO AVANT VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 16, 2013

    TIBIAL COMPONENT PRECOAT RIGHT MEDIAL/LEFT LATERAL SIZE 3

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSX·February 3, 2017

    ZEPHYR XL DR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·April 3, 2013

    X7000 XENON LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·March 22, 2011

    SHILEY TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·NELLCOR/TYCO HEALTHCARE·Product code BTO·April 23, 2008

    C20441 IL HAIFA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·March 28, 2012

    SMALL SUPERIOR AUGMENT GLENOID PLATE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 27, 2024