BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    MICRO DYNAMIC MESH

    FDA 510(k)
    FDA Class 2 ·Dental

    SeeMore Software

    FDA UDI
    INTERSON CORP·00850921007165·SeeMore Software 4.2.1 Urology

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    FDA UDI
    INTERSON CORP·00850921007158·SeeMore Software 4.2.1 Generic

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    FDA UDI
    INTERSON CORP·00850921007141·SeeMore Software 4.2.1 OB GYN

    OTICON I22P CUSTOM FULL CONCHA (ITE) HRNG AID

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    SMITH & NEPHEW BIPOLAR ADAPTER CABLE, MODEL 72200022

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·June 26, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·February 28, 2013

    DIMENSION® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code MMI·February 10, 2011

    BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·June 3, 2016