BEUDAMED
    8 results · 23ms · 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 ×

    HEARTLIGHT

    FDA Adverse Event
    Injury ·CARDIOFOCUS·Product code OAE·November 26, 2018

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 30, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    LIKORALL

    FDA Adverse Event
    Other ·LIKO AB·Product code FSA·August 29, 2008

    G-ARMOR COVERED STENT

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code PNF·January 17, 2023

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016