BEUDAMED
    4,048 results · 72ms · 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.

    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 MEDICAL INSTRUMENTS,INC.

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·August 26, 2015

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 17, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 24, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 5, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·COSTA MESA MFG DC·Product code CBK·April 26, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·COSTA MESA MFG DC·Product code CBK·May 17, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Malfunction ·NEWPOT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 24, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 5, 2017

    NEWPORT MEDICAL INSTRUMENTS, INC.

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·October 23, 2015

    3003135857-2006-00032

    FDA Adverse Event
    Malfunction ·Product code CBK·June 1, 2006

    3003135857-2008-00006

    FDA Adverse Event
    Malfunction ·Product code CBK·February 5, 2008

    3003135857-2008-00007

    FDA Adverse Event
    Malfunction ·Product code CBK·February 5, 2008

    3003135857-2007-00004

    FDA Adverse Event
    Malfunction ·Product code CBK·February 15, 2007

    3003135857-2007-00030

    FDA Adverse Event
    Product code CBK·June 27, 2007

    3003135857-2007-00028

    FDA Adverse Event
    Product code CBK·June 27, 2007

    3003135857-2007-00025

    FDA Adverse Event
    Malfunction ·Product code CBK·May 24, 2007

    3003135857-2007-00024

    FDA Adverse Event
    Product code CBK·June 1, 2007

    3003135857-2006-00050

    FDA Adverse Event
    Malfunction ·Product code CBK·October 25, 2006