BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    SURGICAL LASER ACCESSORIES (SLA) CASE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    IQM Integral Quality Monitor (also IQM)

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERI-SLEEVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MIH·January 6, 2021

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·June 10, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 8, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·December 10, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 11, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·April 25, 2017

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MIH·January 5, 2021