BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    FLEXCATH STEERABLE SHEATH & DILATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Cordant

    FDA UDI
    Seaspine Orthopedics Corporation·10889981115302·57mm

    EZ CONNECT RESIN

    FDA 510(k)
    FDA Class 2 ·Dental

    800 SERIES EASYNEB NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 25, 2025

    OMNIGUIDE BEAMPATH FIBER AND ADAPTER

    FDA Adverse Event
    OMNIGUIDE, INC.·Product code GEX·October 19, 2010

    ASR TAP SLV ADAP 12/14 -1

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·March 17, 2016

    UNKNOWN NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·April 22, 2013

    GO BED PLUS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 18, 2011

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·June 30, 2008