BEUDAMED
    501 results · 29ms · 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 FDA Adverse Event ×

    INTELLIVUE PATIENT MONITOR MX750

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·December 22, 2025

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS NORTH AMERICA LLC·Product code MHX·July 20, 2021

    INTELLIVUE MULTI MEASUREMENT SERVER X2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DSI·May 30, 2025

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·January 12, 2012

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·October 10, 2025

    INTELLIVUE MP50

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DSI·October 24, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code FRN·May 8, 2026

    INTELLIVUE MX800 PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·February 23, 2026

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·January 12, 2012

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 8, 2025

    INTELLIVUE PATIENT MONITOR MX700

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·May 12, 2026

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 30, 2026

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS NORTH AMERICA LLC·Product code MHX·January 11, 2022

    BIOROOT RCS

    FDA Adverse Event
    Injury ·SEPTODONT, INC.·Product code KIF·October 23, 2017

    BIOROOT RCS

    FDA Adverse Event
    Injury ·SEPTODONT SAS·Product code KIF·August 28, 2023

    BIOROOT RCS

    FDA Adverse Event
    Injury ·SEPTODONT, INC.·Product code KIF·July 4, 2017

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 18, 2020

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·April 13, 2026

    INTELLIVUE MX40 1.4GHZ

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·February 10, 2026

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 19, 2025