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

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    LIGHTCAST II STOCKINETTE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209137855·

    MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Reperen Surgical Mesh

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 8, 2022

    RENASYS EZ PLUS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW WOUND MANAGEMENT·Product code BTA·April 24, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·September 28, 2012

    PAD CONNECTOR CABLE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 21, 2010