BEUDAMED
    18 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Malfunction ·FLIGHT MEDICAL LTD.·Product code CBK·November 15, 2005

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Malfunction ·FLIGHT MEDICAL LTD.·Product code CBK·November 15, 2005

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Malfunction ·FLIGHT MEDICAL LTD.·Product code CBK·November 15, 2005

    HT50-H1B

    FDA Adverse Event
    Other ·*·Product code CBK·May 30, 2008

    2023050-2008-00077

    FDA Adverse Event
    Malfunction ·Product code CBK·November 11, 2008

    2023050-2007-00009

    FDA Adverse Event
    Malfunction ·Product code CBK·March 9, 2007

    2023050-2017-05006

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·February 21, 2017

    2023050-2017-05005

    FDA Adverse Event
    Injury ·COSTA MESA MFG DC·Product code CBK·February 21, 2017

    HT50 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·April 7, 2017

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·April 7, 2017

    HT50 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·April 12, 2017

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·April 12, 2017

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Death ·FLIGHT MEDICAL LTD.·Product code CBK·May 19, 2006

    NEWPORT HT50 VENTILATOR

    FDA Adverse Event
    Death ·FLIGHT MEDICAL LTD.·Product code CBK·May 19, 2006

    CAPSURE Z NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·March 27, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 24, 2011

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008

    EVIS EXERA ¿ GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·October 6, 2021