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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    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

    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

    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