BEUDAMED
    3,811 results · 29ms · Sources: EU EUDAMED, US FDA

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    DPM 7 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    TEMPUS LS-MANUAL

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·October 9, 2024

    3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL INC.·Product code LSZ·May 14, 2022

    DPM 5 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·April 30, 2013

    DPM 6/7 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    TEMPUS LS-MANUAL

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·June 26, 2024

    TEMPUS LS-MANUAL

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·January 18, 2024

    TEMPUS LS-MANUAL

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·November 21, 2023

    DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485 for use with Mindray DPM 6 and DPM 7 patient monitors . Intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters.

    FDA Recall
    Terminated ·Mindray DS USA, Inc. dba Mindray North America·Product code MHX·October 6, 2014

    DPM 6 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 1, 2013

    DPM 5

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·May 21, 2013

    DPM 6 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code DSI·April 30, 2013

    TEMPUS LS

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·February 6, 2024

    TEMPUS LS

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code LDD·November 4, 2024

    DPM 5

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·March 8, 2013

    DPM 6

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·May 21, 2013

    DPM 6

    FDA Adverse Event
    MINDRAY DS USA, INC.·Product code MHX·May 21, 2013

    DPM 6

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·May 21, 2013

    DPM 6

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·May 21, 2013

    DPM 6 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·July 31, 2013