BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Arthrosurface Bone Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GOMCO CIRCUMCISION CLAMP, MOGEN CLAMP, PLASTIBELL CIRCUMCISION DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VITAL SIGNS MONITOR MODEL M3B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SENSIA SR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·October 10, 2014

    GORE DRYSEAL SHEATH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code DYB·May 5, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 14, 2011

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·September 18, 2021