BEUDAMED
    61 results · 51ms · Sources: EU EUDAMED, US FDA

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    VISERA LAPARO-THORACO VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GCJ·February 9, 2018

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·May 27, 2019

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·October 23, 2013

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·October 23, 2019

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·July 24, 2019

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·July 10, 2019

    EVIS EXERA III VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·November 6, 2020

    HD AUTOCLAVABLE CAMERA HEAD

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·April 21, 2021

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 19, 2014

    EVIS EXERA III VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·June 12, 2020

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·August 2, 2019

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·May 27, 2019

    4K CAMERA HEAD

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·August 6, 2020

    EVIS LUCERA COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDF·January 6, 2021

    TEMPA-DOT

    FDA Adverse Event
    Malfunction ·PYMAH CORP.·Product code FQZ·October 10, 1997

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGB·September 18, 2019

    CAMERA HEAD

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·April 26, 2021

    Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.

    FDA Recall
    Terminated ·Integra Limited·Product code HWC·March 1, 2019

    Integra bioBLOCK Resorbable subtaler Implant, 11mm Catalog Number: 040011 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.

    FDA Recall
    Terminated ·Integra Limited·Product code HWC·March 1, 2019

    Integra bioBLOCK Resorbable subtaler Implant, 12mm Catalog Number: 040012 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.

    FDA Recall
    Terminated ·Integra Limited·Product code HWC·March 1, 2019