BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SOLETRA

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code MHY·November 27, 2012

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011

    BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·October 18, 2017

    BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·October 18, 2017

    BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·October 18, 2017

    BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·October 18, 2017