BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    TEXAS INTERFACE PRESSURE EVALUATOR-TIPE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9

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

    SOLARC/SOLRX 500 SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY A NEW MEDICAL DEVICE FAMILY CONSISTING OF 5 MODELS:

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

    PRIDE MOBILITY PRODUCTS

    FDA Adverse Event
    Injury ·PRIDE MOBILITY PRODUCTS·Product code ITI·May 27, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·November 14, 2012

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·September 8, 2010