BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    IRRIJET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023925·PADDLE SPREADER, 9MM

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0102090·Shaver, Open 9mm

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127020407·Neck Trial, Size 9, Lateral

    ELECTRO-NERVE STIMULATOR TENS, MODEL HE-DIGITAL

    FDA 510(k)
    FDA Class 2 ·Neurology

    Diazyme 1,5-AG Assay

    FDA 510(k)
    FDA Class 2 ·Hematology

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·February 4, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 9, 2007

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 31, 2012

    MICRUSPHERE XL 6MMX20CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·November 20, 2020