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

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    Filters FDA Adverse Event ×

    PURITAN BENNETT 980 SERIES VENTILATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·June 6, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·July 14, 2011

    TAMPONADE URETERINE BALLOON CATHETER SET

    FDA Adverse Event
    Injury ·COOK UROLOGICAL·Product code KNA·October 16, 2007