BEUDAMED
    22 results · 27ms · 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 ×

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 8, 2020

    HEARTMATE GOGEAR SHOWER BAG

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 19, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·December 20, 2019

    HEARTMATE SYSTEM MONITOR

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 2, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·December 13, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 19, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 27, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·July 16, 2018

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 13, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·March 29, 2021

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·March 27, 2021

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·December 13, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 27, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·December 27, 2019

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 29, 2020

    STRATA II VALVE, REGULAR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·April 11, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 15, 2011

    CELL DYN SAPPHIRE ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·June 12, 2008

    COBAS TAQMAN HCV TEST, V2.0 FOR USE WITH THE HIGH PURE SYSTEM CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MZP·May 3, 2012

    COBAS AMPLIPREP / COBAS TAQMAN HCV, CE-IVD

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS·Product code MZP·July 9, 2012