BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    UMBILI-CATH

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 23, 2010

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 16, 2013

    AXIOM ARISTOS FX

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. CX-RU US QT·Product code KPR·July 8, 2014

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 2, 2019