BEUDAMED
    16 results · 78ms · Sources: EU EUDAMED, US FDA

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    Medical Intelligence Medizintechnik GmbH

    Manufacturer
    🇩🇪 Germany

    IGUIDE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code IYE·April 14, 2014

    HEXAPOD EVO RT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code JAI·March 26, 2014

    HEXAPOD EVO RT SYSTEM

    FDA Adverse Event
    MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code JAI·February 21, 2014

    IBEAM

    FDA Adverse Event
    Other ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code IXQ·August 5, 2011

    BODYFIX

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code LHN·May 5, 2006

    HEXAPOD

    FDA Adverse Event
    Other ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code JAI·April 22, 2008

    IBEAM

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code JAI·July 26, 2006

    IBEAM

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code JAI·July 26, 2006

    IBEAM

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code JAI·July 26, 2006

    IBEAM

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK-GMBH·Product code JAI·July 26, 2006

    CONNEXION IMAGING MODULE

    FDA Adverse Event
    Malfunction ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code IXQ·April 10, 2018

    IGUIDE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code IYE·June 12, 2017

    HEADFIX

    FDA Adverse Event
    Injury ·MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH·Product code IYE·August 19, 2010

    IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.

    FDA Enforcement
    Class II ·Terminated·Medical Intelligence Medizintechnik Gmbh·July 31, 2019

    IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.

    FDA Recall
    Terminated ·Medical Intelligence Medizintechnik Gmbh Robert-bosch-str. 8 Schwabmunchen Germany·Product code IYE·July 18, 2019