BEUDAMED
    20 results · 68ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    V24/26 COMPONENT MONITORING SYSTEM

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·October 2, 2003

    4 WAVE MONITOR

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·August 22, 2003

    IMAGEPOINT

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code IYN·September 22, 2000

    HEWITT-PACKER/AGILENT

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES INC.·Product code MLN·September 27, 2000

    FLEX MONOCLONAL RABBIT ANTI-HUMAN ESTROGEN RECEPTOR CLONE EP1

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC·Product code NJT·May 22, 2026

    AGILENT INFO CENTER

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·March 3, 2003

    COMPONENT MONITORING SYSTEM

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·December 8, 2000

    HEART START XL

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code MKJ·May 13, 2013

    VIRIDIA 26/24 COMPONENT MONITORING SYSTEM

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·January 5, 2000

    AGILENT TECHNOLOGIES

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code CCK·March 16, 2001

    AGILENT TECHNOLOGIES

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC·Product code DRT·January 8, 2001

    AGILENT INFORMATION CENTER

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·March 30, 2001

    AGILENT 7000 C GC/MS TRIPLE QUAD

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES INC.·Product code DOP·June 13, 2023

    TRANSPORT MONITOR

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code MHX·November 18, 1999

    ECG LIMB CLAMP ELECTRODES

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC·Product code DRX·July 7, 2008

    CCM ARRHYTHMIA DETECTION OPTION

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code DRT·September 21, 2005

    COMPONENT CENTRAL MONITOR

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC·Product code MHX·May 10, 2002

    TRANSESOPHAGEAL ENDOSCOPIC (TEE) PROBE

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code ITX·June 15, 2001

    TRANSESOPHAGEAL ENDOSCOPIC (TEE) PROBE

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES, INC.·Product code ITX·August 28, 2001

    PORTABLE PATIENT MONITOR

    FDA Adverse Event
    Injury ·AGILENT TECHNOLOGIES INC·Product code MHX·August 29, 2001