BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SELOX SR 53

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO·Product code DTB·June 29, 2006

    SELOX SR 60

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DTB·June 29, 2006

    LIFETEC ELITE V1.0

    FDA Adverse Event
    Malfunction ·IT SYNERGISTICS, LLC·Product code MMH·July 29, 2016

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 19, 2013

    COGNIS

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

    LAB-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)

    FDA Adverse Event
    Malfunction ·COSTA RICA·Product code LTI·June 10, 2008

    ARIS TRANSOBTURATOR KIT

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code OTN·September 9, 2021